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| Product | Description | |
|---|---|---|
| 1,10-Phenanthroline Nickel dibromide | 1,10-Phenanthroline Nickel dibromide is a Ni precatalyst used for a variety of cross-coupling reactions, including N-alkylation of amides and arylation of alcohols. Uses: Transition metal catalysts. Synonyms: Nickel, dibromo(1,10-phenanthroline-κN1,κN10)-; Dibromo(1,10-phenanthroline-κN1,κN10)nickel; Nickel, dibromo(1,10-phenanthroline)-; Nickel, dibromo(1,10-phenanthroline-N1,N10)-; Dibromo(1,10-phenanthroline-κN1,κN10)nickel; 1,10-Phenanthroline nickel (II) dibromide; Ni (phen) Br2; (phen)NiBr2. Grades: ≥95%. CAS No. 48165-50-0. Molecular formula: C12H8Br2N2Ni. Mole weight: 398.71. |  |
| 1,10-Phenanthroline Nickel dichloride | . Uses: Transition metal catalysts. Synonyms: (T-4)-Dichloro(1,10-phenanthroline-κN1,κN10)nickel; Nickel, dichloro(1,10-phenanthroline-κN1,κN10)-, (T-4)-; Nickel, dichloro(1,10-phenanthroline)-; Nickel, dichloro(1,10-phenanthroline-N1,N10)-, (T-4)-; (1,10-Phenanthroline)dichloronickel; Dichloro(1,10-phenanthroline)nickel; Ni(phen)Cl2; phenNiCl2; 1,10-Phenanthroline nickel (II) dichloride. Grades: ≥95%. CAS No. 22980-76-3. Molecular formula: C12H8Cl2N2Ni. Mole weight: 309.80. | |
| [1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene]triphenylphosphine Nickel(II) Dichloride | [1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene]triphenylphosphine Nickel(II) Dichloride. Group: Polymerization catalystspolymerization reagents. Alternative Names: ANW-39473; TR-038322; ACMC-209r5v; DTXSID70718746; 903592-98-3; AKOS015833437. CAS No. 903592-98-3. Product ID: [1,3-bis[2,6-di(propan-2-yl)phenyl]imidazol-2-ylidene]-triphenyl-λ5-phosphane; dichloronickel. Molecular formula: 780.48. Mole weight: C45H51Cl2N2NiP. CC (C)C1=C (C (=CC=C1)C (C)C)N2C=CN (C2=P (C3=CC=CC=C3) (C4=CC=CC=C4)C5=CC=CC=C5)C6=C (C=CC=C6C (C)C)C (C)C. Cl[Ni]Cl. InChI=1S/C45H51N2P. 2ClH. Ni/c1-32 (2) 39-26-18-27-40 (33 (3) 4) 43 (39) 46-30-31-47 (44-41 (34 (5) 6) 28-19-29-42 (44) 35 (7) 8) 45 (46) 48 (36-20-12-9-13-21-36, 37-22-14-10-15-23-37) 38-24-16-11-17-25-38; ; ; /h9-35H, 1-8H3; 2*1H; /q; ; ; +2/p-2. IGLKEXXECLLIAD-UHFFFAOYSA-L. |  |
| 2,2'-Bipyridine Nickel(II) dibromide | . Uses: Transition metal catalysts. Synonyms: Nickel, (2,2'-bipyridine-κN1,κN1')dibromo-, (SP-4-2)-; Nickel, (2,2'-bipyridine)dibromo-; Nickel, (2,2'-bipyridine-N,N')dibromo-, (SP-4-2)-; (2,2'-Bipyridine)dibromonickel; (2,2'-Bipyridine)nickel dibromide; Ni(bpy)Br2; Nibr2(bipy). Grades: ≥95%. CAS No. 46389-47-3. Molecular formula: C10H8Br2N2Ni. Mole weight: 374.68. | |
| 2,2'-Bipyridine Nickel(II) dichloride | . Uses: Transition metal catalysts. Synonyms: Ni(bpy)Cl2; Nickel, (2,2'-bipyridine-κN1,κN1')dichloro-, (SP-4-2)-; Nickel, (2,2'-bipyridine)dichloro-; Nickel, (2,2'-bipyridine-N,N')dichloro-; (2,2'-Bipyridine)dichloronickel; (2,2'-Bipyridine)nickel dichloride; Dichloro(2,2'-bipyridine)nickel; [Bipyridine]nickel(II) dichloride. Grades: ≥95%. CAS No. 22775-90-2. Molecular formula: C10H8Cl2N2Ni. Mole weight: 285.78. | |
| 2,2'-Bipyridine Nickel(II) diiodide | . Uses: Transition metal catalysts. Synonyms: Nickel, (2,2'-bipyridine-κN1,κN1')diiodo-, (SP-4-2)-; Nickel, (2,2'-bipyridine-N,N')diiodo-, (SP-4-2)-; Nickel, (2,2'-bipyridine)diiodo-; (2,2'-Bipyridine)diiodonickel; (2,2'-Bipyridine)diiodonickel(II); (bpy)NiI2. Grades: ≥95%. CAS No. 59448-25-8. Molecular formula: C10H8I2N2Ni. Mole weight: 468.69. | |
| (2,2'-bis(Diphenylphosphino)-1,1'-binaphthyl) Nickel(II) bromide | . Uses: Transition metal catalysts. Synonyms: Nickel, [[1,1'-binaphthalene]-2,2'-diylbis[diphenylphosphine-κP]]dibromo-, (SP-4-2)-. Grades: ≥95%. CAS No. 291278-93-8. Molecular formula: C44H32Br2NiP2. Mole weight: 841.17. | |
| 2,3-Bis(2,6-diisopropylphenylimino)butane | 1. Ligand used in the preparation of highly active metal catalysts for the polymerization of ethylene (ref 1, M=Ni, Pd) and olefins (ref 2, M=Pd; ref 3, M= Hf, Zr) Ligand for the iron catalyzed polymerization of styrene acrylate monomers Ligand for Yttrium complex that catalysis the ring-opening polymerization of cyclic esters Ligand for rare-earth dichloro and bis(alkyl) complexes for isoprene polymerization Ligand for cobalt catalyzed alkene hydroboration Ligand for nickel catalyzed alkene hydrosilylation. Group: Heterocyclic organic compound. Alternative Names: N-(2,6-diisopropylphenyl)-N-{2-[(2,6-diisopropylphenyl)imino]-1-methylpropylidene}amine; N-((E,2E)-2-[(2,6-Diisopropylphenyl)imino]-1-methylpropylidene)-2,6-diisopropylaniline #; TRA0127768; N,N inverted exclamation marka-Bis(2,6-diisopropylphenyl)-2,3-butanediimine; J-400165; AKOS025295710; N2,N3-bis[2,6-di(propan-2-yl)phenyl]butane-2,3-diimine; (N,N'E,N,N'E)-N,N'-(butane-2,3-diylidene)bis(2,6-diisopropylaniline); 74663-77-7; ZINC15230312. CAS No. 74663-77-7. Molecular formula: C28H40N2. Mole weight: 404.642g/mol. IUPACName: 2-N,3-N-bis[2,6-di(propan-2-yl)phenyl]butane-2,3-diimine. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N=C (C)C (=NC2=C (C=CC=C2C (C)C)C (C)C)C. Catalog: ACM74663777. |  |
| 2,6-Bis(N-pyrazolyl)pyridine Nickel(II) dichloride | 2,6-Bis(N-pyrazolyl)pyridine nickel (II) dichloride is a Ni precatalyst that can be used in Negishi alkyl-alkyl cross-coupling, reductive cross-coupling of styrenyl aziridines, and dialkyl ether formation. Uses: Transition metal catalysts. Synonyms: Nickel, dichloro[2,6-di(1H-pyrazol-1-yl-κN2)pyridine-κN]-; (bpp)NiCl2. Grades: ≥95%. CAS No. 2304667-33-0. Molecular formula: C11H9Cl2N5Ni. Mole weight: 340.82. | |
| 3,4,7,8-Tetramethyl-1,10-phenanthroline Nickel (II) dichloride | 3,4,7,8-Tetramethyl-1,10-phenanthroline Nickel (II) dichloride is a Ni catalyst used for a variety of cross-coupling reactions including the cross-electrophile coupling of benzyl alcohols and aryl halides. Uses: Transition metal catalysts. Synonyms: Nickel, dichloro(3,4,7,8-tetramethyl-1,10-phenanthroline-κN1,κN10)-; Dichloro(3,4,7,8-tetramethyl-1,10-phenanthroline-κN1,κN10)nickel; (Me4Phen)NiCl2. Grades: ≥95%. CAS No. 2254430-88-9. Molecular formula: C16H16Cl2N2Ni. Mole weight: 365.91. | |
| 4,4'-Dimethoxy-2,2'-bipyridine Nickel(II) dibromide | . Uses: Transition metal catalysts. Synonyms: Nickel, dibromo(4,4'-dimethoxy-2,2'-bipyridine-κN1,κN1')-; Dibromo(4,4'-dimethoxy-2,2'-bipyridine-κN1,κN1')Nickel; (4,4'-dMeObpy)NiBr2. Grades: ≥95%. CAS No. 2409691-04-7. Molecular formula: C12H12Br2N2NiO2. Mole weight: 434.74. | |
| 4,4'-di-tert-Butyl-2,2'-bipyridine Nickel(II) dibromide | . Uses: Transition metal catalysts. Synonyms: Nickel, [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']dibromo-, (T-4)-; (Dtpby)NiBr2; Dibromo(4,4'-di-tert-butyl-2,2'-bipyridine)nickel; NiBr2(dtbbpy); (SP-4-2)-[4,4'-Bis(1,1-dimethylethyl)-2,2'-bipyridine-kappan1,kappan1']dibromo-nickel; Nickel, [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']dibromo-, (SP-4-2)-; 4,4'-Bis(tert-butyl)-2,2'-bipyridine]nickel Dibromide. Grades: ≥95%. CAS No. 1894189-67-3. Molecular formula: C18H24Br2N2Ni. Mole weight: 486.90. | |
| 4,4'-di-tert-Butyl-2,2'-bipyridine Nickel(II) dichloride | . Uses: Transition metal catalysts. Synonyms: Nickel, [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']dichloro-, (SP-4-2)-; Dichloro(4,4'-di-tert-butyl-2,2'-bipyridine)nickel; [4,4'-Bis(1,1-dimethylethyl)-2,2'-bipyridine] nickel (II) dichloride; (4,4'-dtbbpy)NiCl2. Grades: ≥95%. CAS No. 1034901-50-2. Molecular formula: C18H24Cl2N2Ni. Mole weight: 398.00. | |
| (4,4'-dMeObpy)NiCl2 | . Uses: Transition metal catalysts. Synonyms: 4,4'-Dimethoxy-2,2'-bipyridine nickel (II) chloride; Nickel, dichloro(4,4'-dimethoxy-2,2'-bipyridine-κN1,κN1')-; Dichloro(4,4'-dimethoxy-2,2'-bipyridine-κN1,κN1')-Nickel; 4,4'-dimethoxy-2,2'-bipyridine Nickel dichloride. Grades: ≥95%. CAS No. 1303613-81-1. Molecular formula: C12H12Cl2N2NiO2. Mole weight: 345.84. | |
| 4-Methoxypicolinimidamide hydrochloride | Nickel Catalysts. Alternative Names: 4-methoxypyridine-2-carboximidamide hydrochloride; 4-METHOXYPICOLINIMIDAMIDE HCL; TC-067633; SC-54062; AX8242371; MFCD12755550; W-3930. CAS No. 1179361-66-0. Molecular formula: C7H10ClN3O. Mole weight: 187.627g/mol. IUPACName: 4-methoxypyridine-2-carboximidamide;hydrochloride. Canonical SMILES: COC1=CC(=NC=C1)C(=N)N.Cl. Catalog: ACM1179361660. | |
| Ammonium Nickel(II)Sulfate Hexahydrate | Ammonium Nickel(II)Sulfate Hexahydrate can act as a new ultraviolet light filter. In addition, they serve as catalysts in the preparation of mesocale-ordered conductin polymers. Group: Biochemicals. Grades: Highly Purified. CAS No. 7785-20-8. Pack Sizes: 25g, 50g. Molecular Formula: H8N2NiO8S2 6(H2O), Molecular Weight: 286.906180199999. US Biological Life Sciences. |  Worldwide |
| Bis(4-methylpyridine) Nickel dibromide | . Uses: Transition metal catalysts. Synonyms: Nickel, dibromobis(4-methylpyridine)-; Dibromobis(4-methylpyridine)nickel; Nickel, dibromobis(4-picoline)-; Dibromobis(γ-picoline)nickel. Grades: ≥95%. CAS No. 14650-93-2. Molecular formula: C12H14Br2N2Ni. Mole weight: 404.75. | |
| Bis[η-(2,5-norbornadiene)]rhodium(I) Tetrafluoroborate | Bis{P,P'-1,5-diphenyl-3,7-bis[(4-hydrogenphosphonate)phenyl]-1,5,3,7-diazadiphosphocine} nickel(II) bromide (hydrogen bromide adduct) can be used as Synthetic nickel catalyst used for photocatalytic reduction of aqueous protons to hydrogen and catalyst containing phosphonate anchor groups for immobilation on metal oxide semiconductor surfaces, enabling light-driven hydrogen evolution. Group: Rhodium series of catalysts. Alternative Names: 36620-11-8; Bis(norbornadiene)rhodium(I) tetrafluoroborate; [rh(nbd)2]bf4; SC-49716; Bis(bicyclo[2.2.1]hepta-2,5-diene)rhodium tetrafluoroborate; ANW-41403; MFCD00671775; Bis (norbornadiene) (tetrafluoroborato)rhodium; bis(norbomadiene)rhodium (I) tetrafluoroborate; Bis(norbornadiene)rhodium (I) tetrafluoroborate. CAS No. 36620-11-8. Molecular formula: C14H16BF4Rh-. Mole weight: 373.991g/mol. IUPACName: bicyclo[2.2.1]hepta-2,5-diene;rhodium;tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F. C1C2C=CC1C=C2. C1C2C=CC1C=C2. [Rh]. Catalog: ACM36620118. | |
| Bis (hexafluoroacetylacetonato)nickel (II) hydrate | . Uses: Transition metal catalysts. Synonyms: Nickel, bis(1,1,1,5,5,5-hexafluoro-2,4-pentanedionato-κO,κO')-, hydrate, (SP-4-1)-; Bis(1,1,1,5,5,5-hexafluoro-2,4-pentanedionato)nickel hydrate; Hexafluoroacetylacetono nickel(II) salt hydrate; Nickel(II) Hexafluoroacetylacetonate hydrate. Grades: ≥95%. CAS No. 207569-13-9. Molecular formula: C10H2F12NiO4.xH2O. Mole weight: 472.80 (anhydrous basis). | |
| Bis{P,P'-1,5-diphenyl-3,7-bis[(4-hydrogenphosphonate)phenyl]-1,5,3,7-diazadiphosphocine} nickel(II) bromide (hydrogen bromide adduct) | 1. Synthetic nickel catalyst used for photocatalytic reduction of aqueous protons to hydrogen. 2. Catalyst containing phosphonate anchor groups for immobilation on metal oxide semiconductor surfaces, enabling light-driven hydrogen evolution. Group: Nickel catalysts. Alternative Names: [4-[3, 7-Diphenyl-5-[4-(phosphonatomethyl)phenyl]-1, 5, 3, 7-diazadiphosphocane-3, 7-diium-1-yl]phenyl]methyl-dioxido-oxo-lambda5-phosphane; hydron; nickel(2+); trihydrobromide. CAS No. 1514896-39-9. Molecular formula: C60H73Br3N4NiO12P8. Mole weight: 1588.4. Appearance: Red brown crystal. Purity: 0.98. IUPACName: [4-[3, 7-diphenyl-5-[4-(phosphonatomethyl)phenyl]-1, 5, 3, 7-diazadiphosphocane-3, 7-diium-1-yl]phenyl]methyl-dioxido-oxo-λ 5-phosphane; hydron; nickel(2+); trihydrobromide. Canonical SMILES: [H+]. [H+]. [H+]. [H+]. [H+]. [H+]. C1N (C[PH+] (CN (C[PH+]1C2=CC=CC=C2)C3=CC=C (C=C3)CP (=O) ([O-])[O-])C4=CC=CC=C4)C5=CC=C (C=C5)CP (=O) ([O-])[O-]. C1N (C[PH+] (CN (C[PH+]1C2=CC=CC=C2)C3=CC=C (C=C3)CP (=O) ([O-])[O-])C4=CC=CC=C4)C5=CC=C (C=C5)CP (=O) ([O-])[O-]. [Ni+2]. Br. Br. Br. Catalog: ACM1514896399-1. | |
| Bis(pyridine) Nickel(II) dibromide | . Uses: Transition metal catalysts. Synonyms: Nickel, dibromobis(pyridine)-; Dibromobis(pyridine)nickel. Grades: ≥95%. CAS No. 14024-85-2. Molecular formula: C10H10Br2N2Ni. Mole weight: 376.70. | |
| Bis(triphenylphosphine)(2-methylphenyl) Nickel(II) chloride | Bis(triphenylphosphine)(2-methylphenyl) Nickel(II) chloride is a precursor to the synthesis of an air-stable Ni-precatalyst developed by Buchwald and coworkers. Uses: Transition metal catalysts. Synonyms: Nickel, chloro(2-methylphenyl)bis(triphenylphosphine)-; Chloro (2-methylphenyl)bis (triphenylphosphine)nickel; Nickel, chloro-o-tolylbis(triphenylphosphine)-; Chloro (2-methylphenyl)bis (triphenylphosphine)nickel (II); Buchwald Nickel Cross-Coupling Catalyst Precursor; [Bis(triphenylphosphine)](o-tolyl)chloronickel; Bis(triphenylphosphino)(2-methylphenyl)chloronickel(II). Grades: ≥95%. CAS No. 27057-09-6. Molecular formula: C43H37ClNiP2. Mole weight: 709.85. | |
| Bis(triphenylphosphino)(2-methylphenyl)chloronickel(II), 99% | This complex is used as an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates. This nickel precatalyst is used for the polymerization of halothiophenes. Group: Nickel catalysts. Alternative Names: MFCD28144558; Bis(triphenylphospino)(2-methylphenyl)chloronickel(II); 27057-09-6. CAS No. 27057-09-6. Molecular formula: C43H39ClNiP2+. Mole weight: 711.876g/mol. IUPACName: chloronickel; methylbenzene; triphenylphosphanium. Canonical SMILES: CC1=CC=CC=[C-]1. C1=CC=C (C=C1)[PH+] (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)[PH+] (C2=CC=CC=C2)C3=CC=CC=C3. Cl[Ni]. Catalog: ACM27057096. | |
| Chloro(2-methylphenyl)(N,N,N',N'-tetramethyl-1,2-ethylenediamine)nickel(II), 99% (contains about 5% o-chlorotoluene) NiCl(o-tolyl)(TMEDA) | Air-Stable Nickel precatalyst for cross-coupling Precatalyst allowing various ligands to be used (monoand bidendate phosphines, diimines and NHCs). Group: Nickel catalysts. Alternative Names: Chloro(2-methylphenyl)(N, N, N, N-tetramethyl-1, 2-ethylenediamine)nickel(II); 1702744-45-3; [(TMEDA)Ni(o-tolyl)Cl]; F1905-8610. CAS No. 1702744-45-3. Molecular formula: C13H23ClN2Ni-. Mole weight: 301.484g/mol. IUPACName: chloronickel;methylbenzene;N, N, N', N'-tetramethylethane-1, 2-diamine. Canonical SMILES: CC1=CC=CC=[C-]1.CN(C)CCN(C)C.Cl[Ni]. Catalog: ACM1702744453. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- [bis (4-fluorophenyl] phosphino] ferrocenyl] ethyldi-tert-butylphosphine] nickel (II) | Chloro (4-cyanophenyl) { (R) -1-[ (S) -2- (bis (4-fluorophenyl) phosphinoferrocenyl]ethyl (di-t-butylphosphine) }nickel (II) is used for: 1.Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. 2.Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. 3.Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions. 4.Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-37-3. Mole weight: 774.69. Catalog: ACM2049086373. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldicyclohexylphosphine] nickel (II) | Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions. Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-35-1. Mole weight: 802.88. Catalog: ACM2049086351. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldiphenylphosphine] nickel (II) | Chloro (4-cyanophenyl) { (R) -1-[ (S) -2- (dicyclohexylphosphino) ferrocenyl]ethyl (diphenylphosphine)}nickel(II) is useful in these fields: Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-36-2. Mole weight: 790.79. Catalog: ACM2049086362. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II) | Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II) has the following various uses:1.Versatile, air-stable, low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. 2.Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. 3.Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-34-0. Mole weight: 738.71. Catalog: ACM2049086340. | |
| Chlorobis (dicyclohexylphenylphosphino) (2-methylphenyl)nickel (II), 99% | An air-stable nickel precatalyst for the Internally-selective benzylation of terminal alkenes. Group: Nickel catalysts. CAS No. 1419179-26-2. Molecular formula: C43H61ClNiP2. Mole weight: 734.04. Catalog: ACM1419179262. | |
| cis-[1,2-Bis(diphenylphosphino)ethane](2-methylphenyl)nickel(II) chloride | Nickel Catalysts. CAS No. 1256262-67-5. Mole weight: 583.69. Catalog: ACM1256262675. | |
| Copper Nickel Nanoparticles | Oil & GasNano Catalysts. CAS No. 12357-13-0. Molecular formula: CuNi. Mole weight: 122.239 g/mol. Appearance: Powder. IUPACName: copper; nickel. Canonical SMILES: [Ni].[Cu]. Density: 8.5-8.95 g/cm³. Catalog: ACM12357130-1. | |
| Dichlorobis (dicyclohexylphenylphosphine)nickel (II) | Catalyst used for the coupling of alkenes, aldehydes, and silyl triflates. Catalyst used for the cross-coupling of aryl Grignard reagents with aromatic ethers. Group: Couplingnickel catalysts. Alternative Names: Bis (dicyclohexylphenylphosphino)nickel (II) dichloride. CAS No. 19232-03-2. Molecular formula: C36H56Cl2NiP2. Mole weight: 680.4. Appearance: Orange to brown to dark purple powder to crystal. Purity: 95%+. IUPACName: dichloronickel; dicyclohexyl(phenyl)phosphanium. Canonical SMILES: C1CCC (CC1)[PH+] (C2CCCCC2)C3=CC=CC=C3. C1CCC (CC1)[PH+] (C2CCCCC2)C3=CC=CC=C3. Cl[Ni]Cl. Catalog: ACM19232032-1. | |
| Diglyme Nickel(II) dibromide | . Uses: Transition metal catalysts. Synonyms: Nickel, dibromo[1,1'-(oxy-κO)bis[2-(methoxy-κO)ethane]]-; Dibromo[1,1'-(oxy-κO)bis[2-(methoxy-κO)ethane]]nickel; (2-Methoxyethyl ether)]nickel(II) bromide; Diglyme nickel dibromide; 1-Methoxy-2-(2-methoxyethoxy)ethane dibromonickel (1:1); Nickel(II) bromide 2-methoxyethyl ether complex. Grades: ≥95%. CAS No. 312696-09-6. Molecular formula: C6H14Br2NiO3. Mole weight: 352.67. | |
| Dimethylglyoxime Nickel(II) dichloride | . Uses: Transition metal catalysts. Synonyms: Nickel, [2,3-butanedione di(oxime-κN)]dichloro-; 2,3-Butanedione, dioxime, nickel complex; Nickel, (2,3-butanedione dioxime-N,N')dichloro-; Nickel, (dimethylglyoxime)dichloro-; [2,3-butanedione di(oxime-κN)]dichloro-Nickel. Grades: ≥95%. CAS No. 78147-26-9. Molecular formula: C4H8Cl2N2NiO2. Mole weight: 245.72. | |
| Nickel(II) bis(trifluoromethanesulfonimide) hydrate | Nickel(II) bis(trifluoromethanesulfonimide) hydrate is a compound of utmost importance in the biomedical sector and holds a pivotal role as a catalyst in diverse pharmaceutical procedures. Its catalytic potential enables the synthesis of therapeutics employed for the treatment of neurodegenerative ailments, cancerous conditions, and microbial infections. The exceptional attributes inherent to this compound render it an indispensable constituent in the realm of drug discovery, guaranteeing optimal efficacy and the desired attributes of pharmaceutical agents. Uses: Transition metal catalysts. Synonyms: Nickel, bis[1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl-κO]methanesulfonamidato-κO]-, hydrate (1:x); Nickel bis(trifluoromethylsulfonyl)imide hydrate; Bis[1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl-κO]methanesulfonamidato-κO]nickel hydrate; Bis[bis (trifluoromethylsulfonyl)amino] nickel(II) hydrate. Grades: ≥95%. CAS No. 2067359-93-5. Molecular formula: C4F12N2NiO8S4.xH2O. Mole weight: 618.99 (anhydrous basis). | |
| Nickel(II) bis(trifluoromethylsulfonyl)imide | . Uses: Transition metal catalysts. Synonyms: Nickel bis(trifluoromethylsulfonyl)imide; Nickel, bis[1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl-κO]methanesulfonamidato-κO]-; Bis[1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl-κO]methanesulfonamidato-κO]nickel; Bis[bis (trifluoromethylsulfonyl)amino] nickel(II). Grades: ≥95%. CAS No. 207861-63-0. Molecular formula: C4F12N2NiO8S4. Mole weight: 618.99. | |
| Nickel(II) bromide ethylene glycol dimethyl ether complex | Nickel(II) bromide ethylene glycol dimethyl ether complex is a nickel-based catalyst that is used in the preparation of poly(3-hexylthiophene) (P3HT) Kumada catalyst transfer polymerization. It facilitates good control over the molecular weight of the conjugating polymer. Uses: Transition metal catalysts. Synonyms: Nickel, dibromo[1,2-di(methoxy-κO)ethane]-; Dibromo[1,2-di(methoxy-κO)ethane]nickel; Nickel, dibromo(1,2-dimethoxyethane)-; Nickel, dibromo(1,2-dimethoxyethane-O,O')-; (1,2-Dimethoxyethane)nickel dibromide; 1,2-Dimethoxyethane nickel(II) bromide; Dibromo(1,2-dimethoxyethane)nickel; Dibromo(1,2-dimethoxyethane)nickel(II); Dibromo(glyme)nickel; NiBr2(dme); Nickel(II) dimethoxyethane bromide; Dimethoxyethane Nickel(II) dibromide. Grades: ≥95%. CAS No. 28923-39-9. Molecular formula: C4H10Br2NiO2. Mole weight: 308.62. | |
| Nickel on silica/alumina | Nickel on silica/alumina. Uses: Source of nickel in standards. Group: Fuel cell catalysts. | |
| Nickel peroxide | Nickel Catalysts. Alternative Names: Ni2O3;12035-36-8;Nickel dioxide;8904AF;AKOS015904167;FT-0697412;I14-18082;Nickel peroxide, technical, oxidizing agent, ~30% active peroxide basis. CAS No. 12035-36-8. Molecular formula: Ni2O3. Mole weight: 165.384g/mol. IUPACName: oxo(oxonickeliooxy)nickel. Canonical SMILES: O=[Ni]O[Ni]=O. ECNumber: 234-823-3. Catalog: ACM12035368. | |
| [(S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl] Nickel(II) bromide | . Uses: Transition metal catalysts. Synonyms: Nickel, [(1S)-[1,1'-binaphthalene]-2,2'-diylbis[diphenylphosphine-κP]]dibromo-, (SP-4-2)-. Grades: ≥95%. CAS No. 464894-05-1. Molecular formula: C44H32Br2NiP2. Mole weight: 841.17. | |
| trans-Bis(tricyclohexylphosphine)(2-methylphenyl)nickel(II) chloride | Nickel Catalysts. CAS No. 123839-28-1. Mole weight: 746.13. Catalog: ACM123839281. | |
| Tris(2,2'-bipyridine) Nickel dichloride | . Uses: Transition metal catalysts. Synonyms: Nickel(2+), tris(2,2'-bipyridine-κN1,κN1')-, chloride (1:2), (OC-6-11)-; Nickel(2+), tris(2,2'-bipyridine)-, dichloride; Nickel(2+), tris(2,2'-bipyridine-N,N')-, dichloride, (OC-6-11)-; Nickel(2+), tris(2,2'-bipyridine-κN1,κN1')-, dichloride, (OC-6-11)-; Tris(2,2'-bipyridine)nickel dichloride; Tris(2,2'-bipyridine)nickel(2+) dichloride. Grades: ≥95%. CAS No. 14751-84-9. Molecular formula: C30H24Cl2N6Ni. Mole weight: 598.15. | |
| 1,3-Bis(2,6-Diisopropylphenyl)-4,5-Dihydroimidazolium Tetrafluoroborate | In-situ deprotonation leads to metal carbene species which acts as a catalyst in a variety of C-C and C-N bond forming reactions. Ligand used in the nickel or palladium-catalyzed coupling of aryl chlorides and amines. Ligand used for the palladium-catalyzed arylation of esters and amides. Ligand used for the palladium-catalyzed intermolecular amination of Csp3-H Bonds. Ligand used for the nickel-catalyzed hydrogenation of olefins. Group: Organic phosphine compounds. Alternative Names: 1,3-Bis(2,6-Diisopropylphenyl)-4,5-Dihydro-1H-Imidazol-3-Ium Tetrafluoroborate. CAS No. 282109-83-5. Molecular formula: C27H39BF4N2. Mole weight: 478.4. Appearance: White powder. Purity: 0.98. IUPACName: 1,3-bis[2,6-di(propan-2-yl)phenyl]-4,5-dihydroimidazol-1-ium;tetrafluoroborate. Canonical SMILES: [B-] (F) (F) (F)F. CC (C)C1=C (C (=CC=C1)C (C)C)N2CC[N+] (=C2)C3=C (C=CC=C3C (C)C)C (C)C. Catalog: ACM282109835-1. | |
| [1, 3-Bis (diphenylphosphino) propane]nickel (II) Chloride | [1, 3-Bis (diphenylphosphino) propane]nickel (II) Chloride is used as an effective catalyst for Kumada coupling and Suzuki reactions. It also catalyzes other reactions to convert enol ethers, dithioacetals and vinyl sulfides to olefins. Group: Biochemicals. Grades: Highly Purified. CAS No. 15629-92-2. Pack Sizes: 2.5g, 5g. Molecular Formula: C27H26Cl2NiP2, Molecular Weight: 542.04. US Biological Life Sciences. | Worldwide |
| 2,2':5',2''-TERTHIOPHENE | 2,2':5',2''-Terthiophene (TTh) may be prepared by nickel catalysed coupling reaction of grignard's reagent derived from 2-bromothiophene and magnesium. It generates singlet oxygen. In nature, it is found in the floral extract of Tagetes minuta and Echinops grijisii. It is known to be toxic to mosquitoes. It also exihibits antifungal activity. 2,2':5',2''-Terthiophene (3T) is a tri-thiophene based low band conductive polymer that is prepared by reacting 2,5-dibromothiophene and thienylmagnesium bromide in the presence of nickel catalyst. Uses: 3t can be combined with 3,4-ethylenedioxythiophene (edot) in a tetrabutylammonium perchlorate solution for use as an electrochromic copolymer for a wide range of s like photovoltaics and polymer light emitting diodes (leds). it can also be used to form metal-organic based thin films with metals like aluminum, silver, and calcium which can potentially be used for optoelectronics based s. electroche. Group: other electronic materials synthetic tools and reagents. Alternative Names: 2,5-Di(thien-2-yl)thiophene. CAS No. 1081-34-1. Pack Sizes: Packaging 1 g in glass bottle. Product ID: 2,5-Dithiophen-2-ylthiophene. Molecular formula: 248.4. Mole weight: C12H8S3. C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3. InChI=1S/C12H8S3/c1-3-9 (13-7-1)11-5-6-12 (15-11)10-4-2-8-14-10/h1-8H. KXSFECAJUBPPFE-UHFFFAOYSA-N. 95%+. | |
| Bis(2,4-pentanedionato)nickel(II) Hydrate | Versatile catalyst for polymerization, dimerization, hydrogenation, oxidation and addition reactions. Group: Heterocyclic organic compound. Alternative Names: 120156-44-7;NICKEL(II) ACETYLACETONATE HYDRATE;Acetylacetone nickel(II) salt hydrate; MFCD00149058; C10H14NiO4.H2O; Nickel(II)acetylacetonate hydrate;5718AF;AKOS025311139. CAS No. 120156-44-7. Molecular formula: C10H18NiO5. Mole weight: 276.942g/mol. IUPACName: (Z)-4-hydroxypent-3-en-2-one;nickel;hydrate. Canonical SMILES: CC(=CC(=O)C)O.CC(=CC(=O)C)O.O.[Ni]. Catalog: ACM120156447. | |
| Bis(triphenylphosphine)nickel(II) dichloride | dichloridobis (triphenylphosphane)nickel (II) is a metal phosphine complex with the formula NiCl2[P(C6H5)3]2. It is a dark blue crystalline solid. It is used as a catalyst for organic synthesis. Uses: Ni(pph3)2cl2 may be used to undertake nickel assisted phosphination of biaryl o,n triflates with chlorodiphenylphosphine. Group: Vapor deposition precursorspolymerization reagents. Alternative Names: Dichlorobis (triphenylphosphine)nickel (II), NiCl2(PPh3)2, Nickel(II)bis(triphenylphosphine) dichloride. CAS No. 14264-16-5. Pack Sizes: 10 g in glass bottle. Product ID: dichloronickel; triphenylphosphane. Molecular formula: 654.17. Mole weight: C36H32Cl2NiP2-. Cl[Ni]Cl. c1ccc(cc1)P(c2ccccc2)c3ccccc3. c4ccc(cc4)P(c5ccccc5)c6ccccc6. 1S/2C18H15P. 2ClH. Ni/c2*1-4-10-16 (11-5-1) 19 (17-12-6-2-7-13-17) 18-14-8-3-9-15-18; ; ; /h2*1-15H; 2*1H; /q; ; ; ; +2/p-2, ZBRJXVVKPBZPAN-UHFFFAOYSA-L. ZBRJXVVKPBZPAN-UHFFFAOYSA-L. | |
| BrettPhos | Ligand for palladium-catalyzed cross-coupling reactions using aryl mesylates with electron-deficient anilines. Ligand for palladium-catalyzed cross-coupling of primary arylamines at low catalyst loading. Ligand for palladium-catalyzed cross-coupling of aryl iodides and primary amines. Ligand for the Suziki-Miyaura coupling of tosylates and mesylates. Ligand for the palladium-catalyzed trifluoromethylation of aryl chlorides. Ligand for the palladium-catalyzed formation of aryl-SCF3 compounds from aryl bromides. Ligand for the nickel-catalyzed cross-coupling of styrenyl epoxides with boronic acids. Ligand for the palladium-catalyzed intramolecular CH difluoroalkylation. Group: Organic phosphine compounds. Alternative Names: C35H53O2P; dicyclohexyl-(2',4',6'-triisopropyl-3,6-dimethoxy-biphenyl-2-yl)-phosphane; BrettPhos; 2-(Dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl; ZINC43220891; ST24046493; 2-DICYCLOHEXYLPHOSPHINO-2',4',6'-TRIISOPROPYL-3,6-DIMETHOXYBIPHENYL; AS-19342; 2-(Dicyclohexylphosphino)3,6-dimethoxy-2 inverted exclamation marka,4 inverted exclamation marka,6 inverted exclamation. CAS No. 1070663-78-3. Molecular formula: C35H53O2P. Mole weight: 536.781g/mol. IUPACName: dicyclohexyl-[3,6-dimethoxy-2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane. Canonical SMILES: CC (C)C1=CC (=C (C (=C1)C (C)C)C2=C (C=CC (=C2P (C3CCCCC3)C4CCCCC4)OC)OC)C (C)C. Catalog: ACM1070663783. | |
| Carbonyl Nickel Coated Aluminum Powder (Ni Shell, Al Core) | Carbonyl Nickel Coated Aluminum Powder (Ni Shell, Al Core). Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. | |
| Carbonyl Nickel Iron Alloy Powder | Carbonyl Nickel Iron Alloy Powder. Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Alloys nanopowders. | |
| Carbonyl Nickel Powder (2-3 μm) | Carbonyl Nickel Powder (2-3 μm). Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. CAS No. 8049-31-8. | |
| Carbonyl Nickel Powder (2-3 μm) | Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. CAS No. 8049-31-8. Catalog: ACM8049318. | |
| Carbonyl Nickel Powder (4-7 μm) | Carbonyl Nickel Powder (4-7 μm). Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. CAS No. 8049-31-8. | |
| Nickel Aluminum | Nickel Aluminum is used for preparation of Raney Nickel catalyst. Group: Biochemicals. Grades: Highly Purified. CAS No. 12635-29-9. Pack Sizes: 5g, 10g. Molecular Formula: N/A, Molecular Weight: US Biological Life Sciences. | Worldwide |
| Nickel Aluminum Ni-Al Alloy Powder | Nickel Aluminum Ni-Al Alloy Powder. Uses: Nickel aluminum alloy powder is mainly used in the catalyst hydrogenation reaction of basic organic chemicals. Group: Alloy powders. | |
| Nickel Aluminum, Raney|r type non-activated | 100g Pack Size. Group: Catalysts, Inorganic Chemicals. Formula: AlNi. CAS No. 12635-29-9. Prepack ID 13853276-100g. Molecular Weight 85.67. See USA prepack pricing. |  |
| Nickel Carbonate | Nickel plating, as catalyst for hardening of fats, in ceramic colors & glazes. Group: Nickel plating chemicals. CAS No. 3333-67-3. ECNumber: 222-068-2. Catalog: ACEP3333673. | |
| Nickel(II) acetate tetrahydrate | 100g Pack Size. Group: Catalysts. Formula: C4H6NiO4. CAS No. 6018-89-9. Prepack ID 47116523-100g. Molecular Weight 176.78144. See USA prepack pricing. | |
| Nickel(II) acetylacetonate | Catalyst for organic reactions. Group: Micro/nanoelectronics. Alternative Names: Nickel bis(2,4-pentanedionate). CAS No. 3264-82-2. Molecular formula: C10H16NiO4. Mole weight: 256.91. Appearance: Clear pale yellow liquid. Purity: 95%+. IUPACName: Nickel(2+);(Z)-4-oxopent-2-en-2-olate. Canonical SMILES: CC(=CC(=O)C)[O-]. CC(=CC(=O)C)[O-]. [Ni+2]. Density: 0.145 g/cm³. ECNumber: 221-875-7. Catalog: ACM3264822-2. | |
| Nickel(II) acetylacetonate | Nickel(II) acetylacetonate. Uses: Catalyst for organic reactions. Group: Solution deposition precursors. Alternative Names: Nickel bis(2,4-pentanedionate). CAS No. 3264-82-2. Product ID: Nickel(2+); (Z)-4-oxopent-2-en-2-olate. Molecular formula: 256.91. Mole weight: C10H16NiO4. CC(=CC(=O)C)[O-]. CC(=CC(=O)C)[O-]. [Ni+2]. InChI=1S/2C5H8O2. Ni/c2*1-4(6)3-5(2)7; /h2*3, 6H, 1-2H3; /q; +2/p-2/b2*4-3-. BMGNSKKZFQMGDH-FDGPNNRMSA-L. 95%+. | |
| (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine | Convenient catalyst for the enantioselective borane reduction of ketones at ambient temperatures. Asymmetric synthesis of α-chiral hydroxyalkylphosphines via a catalytic, enantioselective reduction of acylphosphines. Nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: Stereospecific formation of diarylalkanes and triarylmethanes. Enantioselective reduction of prochiral ketones with NaBH4/Me2SO4/(S)-Me-CBS. Group: Other. Alternative Names: AKOS015840981; (S)-1-methyl-3,3-diphenyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole; MFCD00078439; (S)- Methyl-CBS-oxazaborolidine; ZINC169743318; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3 H-pyrrolo[1,2-c][1,3,2] oxazaborole; (S)-1-methyl-3,3-diphenylhexahydropyrrolo-[1,2-c][1,3,2]oxazaborole; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3H-pyrrolo[1,2-c]-[1,3,2]oxazaborole; (S)-Me-CBS; Corey catalyst. CAS No. 112022-81-8. Molecular formula: C18H20BNO. Mole weight: 277.174g/mol. IUPACName: (3aS)-1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole. Canonical SMILES: B1 (N2CCCC2C (O1) (C3=CC=CC=C3)C4=CC=CC=C4)C. Catalog: ACM112022818. | |
| (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine | (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine. Uses: Convenient catalyst for the enantioselective borane reduction of ketones at ambient temperatures. asymmetric synthesis of α-chiral hydroxyalkylphosphines via a catalytic, enantioselective reduction of acylphosphines. nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: stereospecific formation of diarylalkanes and triarylmethanes. enantioselective reduction of prochiral ketones with nabh4/me2so4/(s)-me-cbs. Group: other electronic materials. Alternative Names: AKOS015840981; (S)-1-methyl-3,3-diphenyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole; MFCD00078439; (S)- Methyl-CBS-oxazaborolidine; ZINC169743318; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3 H-pyrrolo[1,2-c][1,3,2] oxazaborole; (S)-1-methyl-3,3-diphenylhexahydropyrrolo-[1,2-c][1,3,2]oxazaborole; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3H-pyrrolo[1,2-c]-[1,3,2]oxazaborole; (S)-Me-CBS; Corey catalyst. CAS No. 112022-81-8. Product ID: (3aS)-1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole. Molecular formula: 277.174g/mol. Mole weight: C18H20BNO. B1 (N2CCCC2C (O1) (C3=CC=CC=C3)C4=CC=CC=C4)C. InChI=1S / C18H20BNO / c1-19-20-14-8-13-17 (20) 18 (21-19, 15-9-4-2-5-10-15) 16-11-6-3-7-12-16 / h2-7, 9-12, 17H, 8, 13-14H2, 1H3 / t17- / m0 / s1. VMKAFJQFKBASMU-KRWDZBQOSA-N. | |
| Skeletal Nickel Catalyst slurry in Water | Skeletal Nickel Catalyst slurry in Water. Group: Biochemicals. Alternative Names: Raney Nickel slurry in Water. Grades: Highly Purified. CAS No. 7440-02-0. Pack Sizes: 25g, 50g, 100g, 250g, 500g. US Biological Life Sciences. | Worldwide |
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