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Product | Description | |
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Ruthenium Red Quick inquiry Where to buy Suppliers range | Ruthenium Red. Group: Biochemicals. Alternative Names: Ammoniated Ruthenium Oxychloride; C.I. 77800; Ruthenium Oxychloride Ammoniated. Grades: Highly Purified. CAS No. 11103-72-3. Pack Sizes: 100mg. Molecular Formula: Cl6H42N14O2Ru3, Molecular Weight: 786.36. US Biological Life Sciences. | Worldwide |
Ruthenium Red Quick inquiry Where to buy Suppliers range | Ruthenium Red. Uses: Ruthenium Red acts as an inhibitor of mitochondrial ETC complexes I and III. Inhibitor of mitochondrial calcium uniporter. Group: Heterocyclic Organic Compound. Alternative Names: AK175476; degrees +/->> AENo>> iE; 11103-72-3; SR-01000076250-2; Ruthenium Red, for microscopy, 85.0-115.0% (calc. on dry basis, AT); MFCD00011479; Ruthenium Red, Technical grade; Ruthenium Red, for microscopy, >=85% (calc. on dry substance, AT). CAS No. 11103-72-3. Molecular formula: Cl6H46N14O2Ru3. Mole weight: 790.374g/mol. IUPAC Name: azane; ruthenium(2+); hexachloride; dihydrate. Exact Mass: 792.918g/mol. SMILES: N.N.N.N.N.N.N.N.N.N.N.N.N.N.O.O.[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Ru+2].[Ru+2].[Ru+2]. InChI: InChI=1S/6ClH.14H3N.2H2O.3Ru/h6*1H; 14*1H3; 2*1H2; ; ; /q; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; 3*+2/p-6. InChIKey: JQJSTVUROJELSR-UHFFFAOYSA-H. H-Bond Donor: 16. H-Bond Acceptor: 22. Monoisotopic Mass: 789.919g/mol. | |
Ruthenium Red Quick inquiry Where to buy Suppliers range | Technical grade. Uses: For analytical and research use. Group: Fluorescence/Luminescence Spectroscopy. CAS No. 11103-72-3. Pack Sizes: 1G, 5G. Mole weight: 786.35. Catalog: AP11103723. Linear Formula: [(NH3)5RuORu(NH3)4ORu(NH3)5]Cl6. | |
1,1?-Bis(dicyclohexylphosphino)ferrocene Quick inquiry Where to buy Suppliers range | Orange-red powder. Uses: Ligand for palladium-catalyzed synthesis of oxindoles by amide ?-arylation. Ligand for palladium-catalyzed alkoxycarbonylation of aryl chlorides. Ligand for ruthenium-catalyzed alcohol-allene C-C coupling reaction via hydrohydroxyalkylation of 1,1-disubstituted allenes employing alcohols. Ligand for nickel-catalyzed cross-coupling reaction of arylboronic acids with aryl carbonates. Ligand for palladium-catalyzed regiodivergent hydroesterification of aryl olefins with phenyl formate to form linear structured phenyl arylpropanoates. Ligand for palladium-catalyzed direct borylation of benzyl alcohol and its analogues in the absence of bases. Group: Organic Phosphine Compounds. Alternative Names: 1,1?-Bis(dicyclohexylphosphino)ferrocene; 1,1-Bis(Dicyclohexylphosphino)Ferrocene; 1,1-BIS(DICYCLOHEXYLPHOSPHINO)FERROCENE. Grades: 98%. CAS No. 146960-90-9. Molecular formula: C34H52FeP2. Mole weight: 578.57. IUPAC Name: dicyclohexyl(cyclopentyl)phosphane; iron. Exact Mass: 578.28900. Melting Point: 134-136ºC. SMILES: C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. [Fe]. InChIKey: LVWMUECONASIMT-UHFFFAOYSA-N. | |
1,2-bis(diphenylphosphino)ethane palladium dichloride, Pd : 18.5 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: This product is widely used in catalyzing the hydrogenation of olefins, the hydrogenation reduction of nitrobenzene, the oxidation of olefins, the carbonylation of olefins with carbon monoxide, and the coupling of Grignard reagents and halogenated hydrocarbons. Group: Colloidal Catalysts. CAS No. 19978-61-1. Molecular Weight: 575.74 g/mol. SMILES: Cl[Pd]Cl. C (CP (c1ccccc1)c2ccccc2)P (c3ccccc3)c4ccccc4. InChI: LDJXFZUGZASGIW-UHFFFAOYSA-L. Boiling Point: 360 °C. Flash Point: 99 %. | |
[1, 3-Bis (2, 6-di-i-propylphenyl) -4, 5-dihydroimidazol-2-ylidene]-[2-i-propoxy-5- (trifluoroacetamido) phenyl]methyleneruthenium (II) dichloride M71-S1Pr Quick inquiry Where to buy Suppliers range | [1, 3-Bis (2, 6-di-i-propylphenyl) -4, 5-dihydroimidazol-2-ylidene]-[2-i-propoxy-5- (trifluoroacetamido) phenyl]methyleneruthenium (II) dichloride M71-S1Pr. Uses: Enhanced activity ruthenium "boomerang" pre-catalyst used in the olefin metathesis, enyne metathesis, and cross metathesis reactions, that can be recycled, and leaves reduced ruthenium in the product after silica gel chromatography. Group: Ruthenium series catalysts. Alternative Names: 1212008-99-5; MFCD12545950; (1, 3-bis (2, 6-diisopropylphenyl) imidazolidin-2-yliden; e) (2-isopropoxy-5- (2, 2, 2-trifluoroacetamido) benzylidene) ruthenium (VI) chloride; [1, 3-Bis (2, 6-di-i-propylphenyl) -4, 5-dihydroimidazol-2-ylidene]-[2-i-propoxy-5- (trifluoroacetamido) phenyl]methyleneruthenium (II) dichloride; [1, 3-Bis (2, 6-di-i-propylphenyl) -4, 5-dihydroimidazol-2-ylidene]-[2-i-propoxy-5- (trifluoroacetamido) phenyl]methyleneruthenium (II) dichloride M71-S1Pr. CAS No. 1212008-99-5. Molecular formula: C39H50Cl2F3N3O2Ru. Mole weight: 821.813g/mol. IUPAC Name: [1, 3-bis[2, 6-di (propan-2-yl) phenyl]imidazolidin-2-ylidene]-dichloro-[[2-propan-2-yloxy-5-[ (2, 2, 2-trifluoroacetyl) amino]phenyl]methylidene]ruthenium. Rotatable Bond Count: 10. Exact Mass: 821.228g/mol. SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N2CCN (C2=[Ru] (=CC3=C (C=CC (=C3)NC (=O)C (F) (F)F)OC (C)C) (Cl)Cl)C4=C (C=CC=C4C (C)C)C (C)C. InChI: InChI=1S/C27H38N2. C12H12F3NO2. 2ClH. Ru/c1-18(2)22-11-9-12-23(19(3)4)26(22)28-15-16-29(17-28)27-24(20(5)6)13-10-14-25(27)21(7)8; 1-7(2)18-10-5-4-9(6-8(10)3)16-11(17)12(13, 14)15; ; ; /h9-14, 18-21H, 15-16H2, 1-8H3; 3-7H, 1-2H3, (H, 16, 17); 2*1H; /q; ; ; ; +2/p-2. InChIKey: UKUOIAIRKSRWAN-UHFFFAOYSA-L. H-Bond Donor: 1. H-Bond Acceptor: 7. Monoisotopic Mass: 821.228g/mol. | |
2-(2-Chlorophenyl)ethanol Quick inquiry Where to buy Suppliers range | 2-(2-Chlorophenyl)ethanol is used in the triethylborane-catalyzed reduction of carbonyl functions to alcohols. 2-(2-Chlorophenyl)ethanol is also used in the preparation of alcohols via ruthenium-catalyzed hydrogenation of carboxylic acids. Group: Biochemicals. Grades: Highly Purified. CAS No. 19819-95-5. Pack Sizes: 1g, 5g. Molecular Formula: C8H9ClO, Molecular Weight: 156.61. US Biological Life Sciences. | Worldwide |
2-Amino-5-nitroso-4,6-pyrimidinediol Quick inquiry Where to buy Suppliers range | 2-Amino-5-nitroso-4,6-pyrimidinediol is used as a reagent in the synthesis of 6-amino-2,3-dimethylpyrimido[4,5-e][1,2,4]triazine-8-one as an inhibitor of dihydropteridine reductase (DHPR). 2-Amino-5-nitroso-4,6-pyrimidinediol is also used in analytical studies for determination of ruthenium and transition metals. Group: Biochemicals. Grades: Highly Purified. CAS No. 55482-22-9. Pack Sizes: 1g, 10g. Molecular Formula: C4H4N4O3, Molecular Weight: 156.1. US Biological Life Sciences. | Worldwide |
Ammonium-nitrido-octachlorodiaquodiruthenate(IV) Quick inquiry Where to buy Suppliers range | red powder. Group: Ruthenium series catalysts. Alternative Names: triammonium diaquaoctachloro-mu-nitridodiruthenate(3-);Ammonium-nitrido-octachlorodiaquodiruthenate(IV). Grades: Ru 34%. CAS No. 27316-90-1. Molecular formula: (NH4)3·Cl8H4NO2Ru2. Mole weight: 589.92. | |
[Bis(pyrazol-1-yl)(acetimino)hydridoborato](p-cymene)ruthenium(II) trifluoromethanesulfonate Quick inquiry Where to buy Suppliers range | [Bis(pyrazol-1-yl)(acetimino)hydridoborato](p-cymene)ruthenium(II) trifluoromethanesulfonate. Uses: Dual site catalyst for the mild, selective nitrile reduction. Alternative Names: MFCD30475645;[Bis(pyrazol-1-yl)(acetimino)hydridoborato](p-cymene)ruthenium(II) trifluoromethanesulfonate;1607436-49-6. CAS No. 1607436-49-6. Molecular formula: C19H26BF3N5O3RuS+. Mole weight: 573.384g/mol. IUPAC Name: di(pyrazol-1-yl)boron; ethanimine; 3-methyl-6-propan-2-ylcyclohexa-1, 4-diene; ruthenium(2+); trifluoromethanesulfonate. Rotatable Bond Count: 3. Exact Mass: 574.084g/mol. SMILES: [B](N1C=CC=N1)N2C=CC=N2. C[C]=N. CC1C=CC(C=C1)C(C)C. C(F)(F)(F)S(=O)(=O)[O-]. [Ru+2]. InChI: InChI=1S/C10H16. C6H6BN4. C2H4N. CHF3O3S. Ru/c1-8(2)10-6-4-9(3)5-7-10; 1-3-8-10(5-1)7-11-6-2-4-9-11; 1-2-3; 2-1(3, 4)8(5, 6)7; /h4-10H, 1-3H3; 1-6H; 3H, 1H3; (H, 5, 6, 7); /q; ; ; ; +2/p-1. InChIKey: WZSBQJNPTYRUOV-UHFFFAOYSA-M. H-Bond Donor: 1. H-Bond Acceptor: 9. Monoisotopic Mass: 574.084g/mol. | |
Borane Ammonia Complex Quick inquiry Where to buy Suppliers range | Borane Ammonia Complex is used as a reducing agent in the synthesis of nanotubes supported by ruthenium nanoparticles. Group: Biochemicals. Grades: Highly Purified. CAS No. 13774-81-7. Pack Sizes: 1g, 2.5g. Molecular Formula: NH3; (BH3), Molecular Weight: 17.03. US Biological Life Sciences. | Worldwide |
Chloro (indenyl)bis (triphenylphosphine)ruthenium (II) Quick inquiry Where to buy Suppliers range | red-brown powder. Group: Ruthenium series catalysts. Grades: 0.98. CAS No. 99897-61-7. Molecular formula: C45H37ClP2Ru. Mole weight: 776.26. IUPAC Name: Chloro (indenyl)bis (triphenylphosphine)ruthenium (II). Exact Mass: 776.11000. Symbol: GHS08. Safty Description: 26-36/37/39. Hazard statements: H351. | |
CORM-3 Quick inquiry Where to buy Suppliers range | CORM-3 is a water-soluble carbon monoxide-releasing molecule with anti-inflammatory and cardioprotective activity. It attenuates NF-κB p65 nuclear translocation, reduces ROS generation and enhances intracellular glutathione and superoxide dismutase levels. Synonyms: Tricarbonylchloro (glycinato)ruthenium; (OC-6-44)-Tricarbonylchloro(glycinato-κN,κO)ruthenium; CORM3; CORM 3. Grades: >98%. CAS No. 475473-26-8. Molecular formula: C5H4ClNO5Ru. Mole weight: 294.61. | |
Dichlorobis (2- (diphenylphosphino) ethylamine) ruthenium (II) Quick inquiry Where to buy Suppliers range | Dichlorobis (2- (diphenylphosphino) ethylamine) ruthenium (II). Uses: Efficient catalyst for the dihydrogen reduction of carboxylic esters and amides to alcohols. Group: Ruthenium series catalysts. Alternative Names: DTXSID30584787; AKOS015900275; Dichlorobis[2- (diphenylphosphino) ethylamine]ruthenium (II) ; dichlorobis[2- (diphenylphosphino) ethylamine]ruthenium (ii); SC10243; 2-(Diphenylphosphanyl)ethan-1-amine--dichlororuthenium (2/1); Dichlorobis (2- (diphenylphosphino) ethylamine) ruthenium (II) , 95%. CAS No. 506417-41-0. Molecular formula: C28H32Cl2N2P2Ru. Mole weight: 630.496g/mol. IUPAC Name: dichlororuthenium;2-diphenylphosphanylethanamine. Rotatable Bond Count: 8. Exact Mass: 630.046g/mol. SMILES: C1=CC=C(C=C1)P(CCN)C2=CC=CC=C2. C1=CC=C(C=C1)P(CCN)C2=CC=CC=C2. Cl[Ru]Cl. InChI: InChI=1S/2C14H16NP.2ClH.Ru/c2*15-11-12-16(13-7-3-1-4-8-13)14-9-5-2-6-10-14;;;/h2*1-10H,11-12,15H2;2*1H;/q;;;;+2/p-2. InChIKey: BJNVYFXBTNBKRU-UHFFFAOYSA-L. H-Bond Donor: 2. H-Bond Acceptor: 2. Monoisotopic Mass: 630.046g/mol. | |
Dichlorodi-μ-chlorobis[(1,2,3,6,7,8-η-2,7-dimethyl-2,6-octadiene-1,8-diyl]diruthenium(IV) Quick inquiry Where to buy Suppliers range | red to purple powder. Uses: Versatile starting material for the preparation of cyclic and acyclic bis(η5 -dienyl)ruthenium (II) compounds. Group: Ruthenium series catalysts. Alternative Names: Tetrachlorobis(2,7-dimethyl-2,6-octadienylene)diruthenium. Grades: 0.98. CAS No. 34801-97-3. Molecular formula: C20H32Cl4Ru2. Mole weight: 616.42. Symbol: GHS07. Melting Point: 193-202 °C (dec.). Safty Description: Warning. Hazard statements: H315-H319-H335. | |
Dichloro (p-cymene)triphenylphosphineruthenium (II) dichloromethane adduct Quick inquiry Where to buy Suppliers range | Dichloro (p-cymene)triphenylphosphineruthenium (II) dichloromethane adduct. Group: Ruthenium Complexes. Alternative Names: Dichloro (p-cymene) (triphenylphosphane)ruthenium (II). Grades: 99%. CAS No. 52490-94-5. Product ID: ACM52490945-1. Molecular formula: C29H31Cl4PRu. Mole weight: 653.41. Appearance: Orange red powder. SMILES: CC1=CC=C (C=C1)C (C)C. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C (Cl)Cl. Cl[Ru]Cl. | |
Dichloro[(R)-(+)-2,2'-bis(diphenylphosphino)-1, 1'-binaphthyl]ruthenium(II) Quick inquiry Where to buy Suppliers range | Dichloro[(R)-(+)-2,2'-bis(diphenylphosphino)-1, 1'-binaphthyl]ruthenium(II). Group: Ruthenium Complexes. Alternative Names: Dichlororuthenium;[1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Grades: 99%. CAS No. 132071-87-5. Product ID: ACM132071875-1. Molecular formula: C44H32Cl2P2Ru. Mole weight: 794.65. Appearance: Brown red powder. SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=CC=C7)C8=CC=CC=C8. Cl[Ru]Cl. | |
Dichlorotris (triphenylphosphine)ruthenium Quick inquiry Where to buy Suppliers range | Dichlorotris (triphenylphosphine)ruthenium. Group: Ruthenium Complexes. Alternative Names: Tris (triphenylphosphine)ruthenium (II) chloride. Grades: 98%. CAS No. 15529-49-4. Product ID: ACM15529494-2. Molecular formula: C54H45Cl2P3Ru. Mole weight: 958.84. Appearance: Reddish brown to black powder. SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. Cl[Ru]Cl. | |
Diiodo(p-cymene)ruthenium(II) dimer Quick inquiry Where to buy Suppliers range | red powder or crystals. Group: Ruthenium series catalysts. Alternative Names: Di-μ-iodo(p-cymene)iodoruthenium(II). Grades: Ru ≥20.0%. CAS No. 90614-07-6. Molecular formula: C20H28I4Ru2. Mole weight: 978.19. Symbol: GHS07. Melting Point: 234-236 °C. Safty Description: Warning. Hazard statements: H302-H319-H412. | |
KP1019 Quick inquiry Where to buy Suppliers range | KP1019, also known as FFC14A, is just the second ruthenium-based anticancer agent after NAMI-A which was developed to the stage of clinical trials. Important steps in the mode of action of KP1019 are thought to be the binding to the serum protein transferrin and the transport into the cell via the transferrin pathway. Additionally, the selective activation by reduction in the tumor might contribute to the low side effects observed in in vivo studies. Apoptosis is induced at non-toxic levels via the mitochondrial pathway. These features distinguish it from the established platinum anticancer drugs and suggest that different types of cancer might be treatable with this drug. Indeed, promising activity against certain types of tumors, which are not successfully treatable with cisplatin, and only a very low incidence of acquired resistance has been observed in in vitro and in vivo studies. Recently, a clinical phase I trial was finished in which none of the treated patients experienced serious side effects, while disease stabilization in five of six evaluable patients was achieved. Synonyms: KP1019; KP 1019; KP-1019; FFC14A; indazolium trans-[tetrachlorobis(1H-indazole)ruthenate(III)]. CAS No. 124875-20-3. Molecular formula: C21H19Cl4N6Ru. Mole weight: 598.30. | |
NAMI-A Quick inquiry Where to buy Suppliers range | NAMI-A is a ruthenium anticancer agent and a metastasis inhibitor. NAMI is an acronym for "New Anti-tumour Metastasis Inhibitor", while the -A suffix indicates that this is the first of a potential series. NAMI-A is a potent agent for the treatment of solid tumor metastases as well as when these tumor lesions are in an advanced stage of growth. NAMI-A is endowed with a mechanism of action unrelated to direct tumor cell cytotoxicity, and such mechanism of action is responsible for a reduced host toxicity. Synonyms: ImH[trans-RuCl4(DMSO)Im]; Na[trans-RuCl(4)(DMSO)Im; Imidazolium trans-imidazoledimethyl sulfoxide-tetrachlororuthenat; Imidazolium-bis (imidazole) di methyl sulfoxideimidazotetrachlororuthenate (III) ; Imidazolium-bis (imidazole) di methyl sulfoxideimidazotetrachlororuthenate (III). Grades: >98%. CAS No. 201653-76-1. Molecular formula: C8H15Cl4N4ORuS. Mole weight: 458.18. | |
(R)-(+)-BINAP Quick inquiry Where to buy Suppliers range | (R)-(+)-BINAP. Uses: (R)-BINAP or (R)-Tol-BINAP can be combined with dichloro(1,5-cyclooctadiene)ruthenium to form precursors to NOYORI CATALYST SYSTEMS. These systems exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. NOYORI CATALYST SYSTEMS have been shown to effect highly enantioselective hydrogenation of functionalized ketones where the substituents are dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester. Useful ligand in asymmetric Heck processes. Ligand employed in palladium-catalyzed asymmetric arylation of ketones. Ligand employed in rhodium-catalyzed 1,4-additions to enones. Ligand employed in palladium-catalyzed hydroamination of styrene derivatives. Ligand employed in silver-catalyzed asymmetric Sakuri-Hosomi allylation and Mukaiyama aldol reaction. Ligand employed in rhodium-catalyzed kinetic resolution of enynes. Ligand employed in asymmetric rhodium-catalyzed hydroboration of cyclopropenes. Ligand employed in silver-catalyzed a-hydroxylation of stannyl enol ethers. Ligand employed in palladium-catalyzed synthesis of chiral allenes. Ligand for palladium-catalyzed enantioselective hetero Michael addition to form b-amino acid derivatives. Ligand employed in rhodium-catalyzed asymmetric rearrangement of alkynyl alkenyl carbinols. Ligand employed in rhodium-catalyzed 1,2-addition of aluminium organyl compounds to cyclic enones. Ligand employed in iridium-catalyzed transfer hydrogenative allylation of benzylic alcohols. Ligand employed in rhodium-catalyzed asymmetric C-Si bond formation by conjugate silyl transfer using a Si-B linkage. Ligand employed in the iridium-catalyzed asymmetric cyclopropane-mediated carbonyl allylation of primary alcohols. Ligand employed in the nickel-catalyzed asymmetric α-arylation of tetralones. Ligand employed in the copper-catalyzed asymmetric propargylation of ketones. Ligand employed in the cobalt-catalyzed asymmetric reductive coupling of alkynes with alkenes. Ligand employed in the rhodium-catalyzed asymmetric 1,4-addition of arylalanes on trisubstituted enones. Ruthenium-catalyzed asymmetric hydrocyanation of imines. Palladium-catalyzed asymmetric intermolecular cyclization. Group: Organic Phosphine Compounds. Alternative Names: -Bis(d | |
RuCl2[(S)-xylbinap][(S)-daipen] Quick inquiry Where to buy Suppliers range | RuCl2[(S)-xylbinap][(S)-daipen]. Uses: Highly active catalyst for hydrogenation of simple ketones giving high enantioselectivity when sterically unsymmetrical ketones such as acetophenone, heteroaryl ketones, benzophenones, cyclopropyl ketones, and cyclohexyl ketones are substrates. Ee's are enhanced with XylBINAP relative to BINAP. The otherwise poorly bonded ketone is held in the transition state by hydrogen bonding to the protic bidentate amine. Carbonyl groups are selectively reduced even when olefins exist in the same molecule. In the presence of strong base, and catalyst, simple ketones, having substituents at the α-position, may be induced to undergo dynamic kinectic resolution during their hydrogenation to produce two chiral carbon centers in high yield. Group: Heterocyclic Organic Compound. Alternative Names: RuCl2[(S)-(DM-BINAP)][(S)-DAIPEN], 220114-01-2, Dichloro[(S)-(-)-2,2 inverted exclamation marka-bis[di(3,5-xylyl)phosphino]-1,1 inverted exclamation marka-binaphthyl][(2S)-(+)-1,1-bis(4-methoxyphenyl)-3-methyl-1,2-butanediamine]ruthenium(II). Grades: 96%. CAS No. 220114-01-2. Molecular formula: C71H74Cl2N2O2P2Ru. Mole weight: 1221.30. IUPAC Name: [ (2S) -1-azanidyl-1, 1-bis (4-methoxyphenyl) -3-methylbutan-2-yl]azanide; [1-[2-bis (3, 5-dimethylphenyl) phosphaniumylnaphthalen-1-yl]naphthalen-2-yl]-bis (3, 5-dimethylphenyl) phosphanium; dichlororuthenium (2+). Exact Mass: 1220.36000. InChIKey: CDEJRZFAUMUTIA-OGLOXHGMSA-N. H-Bond Donor: 2. H-Bond Acceptor: 4. | |
[RuCl(p-cymene)((S)-tolbinap)]Cl Quick inquiry Where to buy Suppliers range | [RuCl(p-cymene)((S)-tolbinap)]Cl. Uses: 1. Useful ligand for palladium-catalyzed carbon-oxygen bond formation. 2. Ligand for palladium-catalyzed α-arylation of ketones. 3. Ligand for Cu-catalyzed asymmetric conjugate reduction. 4. Ligand for Cu-catalyzed asymmetric dienolate addition to aldehydes. 5. Enantioselective conjugate reduction of lactones and lactams. 6. Ligand used in the enantioselective cycloaddition of allenylsilanes with α-Imino esters. 7. Catalytic Aldol reaction to ketones. 8. Ligand with rhodium catalyses [2+2+2] cycloaddition reaction of alkenes and alkynes. 9. Ligand used in the iridium-catalyzed enantioselective C-H bond activation of 2-(alkylamino)-pyridine with alkenes. 10. Iridium-catalyzed regio-, diastereo-, and enantioselective tert-(hydroxyl)-prenylation of alcohols. 11. Rhodium-catalyzed cross cyclotrimerization. Group: Ruthenium series catalysts. Alternative Names: SC10123; (R)-RuCl[(p-cymene)(T-BINAP)]Cl; Chloro[(R)-(+)-2,2 -bis(di-p-tolylphosphino)-1; CHLORO[(S)-(-)-2,2'-BIS(DI-P-TOLYLPHOSPHINO)-1,1'-BINAPHTHYL](P-CYMENE)RUTHENIUM(II) CHLORIDE; MFCD09753014; (S)-RuCl[(p-cymene)(T-BINAP)]Cl; C58H54Cl2P2Ru. CAS No. 228120-95-4. Molecular formula: C58H54Cl2P2Ru. Mole weight: 984.988g/mol. IUPAC Name: [1-[2-bis(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(4-methylphenyl)phosphane; dichlororuthenium; 1-methyl-4-propan-2-ylbenzene. Rotatable Bond Count: 8. Exact Mass: 984.212g/mol. SMILES: CC1=CC=C (C=C1)C (C)C. CC1=CC=C (C=C1)P (C2=CC=C (C=C2)C)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=C (C=C7)C)C8=CC=C (C=C8)C. Cl[Ru]Cl. InChI: InChI=1S/C48H40P2.C10H14.2ClH.Ru/c1-33-13-23-39(24-14-33)49(40-25-15-34(2)16-26-40)45-31-21-37-9-5-7-11-43(37)47(45)48-44-12-8-6-10-38(44)22-32-46(48)50(41-27-17-35(3)18-28-41)42-29-19-36(4)20-30-42;1-8(2)10-6-4-9(3)5-7-10;;;/h5-32H,1-4H3;4-8H,1-3H3;2*1H;/q;;;;+2/p-2. InChIKey: BHIUOOHVIWKUTN-UHFFFAOYSA-L. Monoisotopic Mass: 984.212g/mol. | |
Ruthenium(III) nitrosylchloride Quick inquiry Where to buy Suppliers range | Ruthenium(III) nitrosylchloride. Group: Ruthenium Complexes. Alternative Names: Trichloronitrosylruthenium(IV). Grades: 98%+. CAS No. 18902-42-6. Product ID: ACM18902426-1. Molecular formula: Cl3NORu. Mole weight: 237.43. Appearance: Reddish brown crystal. SMILES: [N-]=O.Cl[Ru](Cl)Cl. | |
Ruthenium(III)nitrosylchloride Quick inquiry Where to buy Suppliers range | red brown crystals. Group: Ruthenium series catalysts. Alternative Names: Trichloronitrosylruthenium(II) monohydrate. Grades: Ru ≥41.5%. CAS No. 18902-42-6. Molecular formula: Ru(NO)Cl3. Mole weight: 237.44. Symbol: GHS07. Safty Description: Warning. Hazard statements: H315-H319-H335. | |
Ruthenium(III) nitrosyl nitrate solution Quick inquiry Where to buy Suppliers range | red-brown liquid. Group: Metal & Ceramic Materials. Alternative Names: RUTHENIUM NITROSO NITRATE;RUTHENIUM (III) NITROSYLNITRATE; TRINITRATONITROSYLRUTHENIUM(II); tris(nitrato-o)nitrosyl-rutheniu; tris(nitrato-O)nitrosylruthenium; RUTHENIUM(III) NITROSYL NITRATE, SOLUTIO N IN DILUTE NITRIC ACID;RUTHENIUM (III) NITROSYL NITRATE S. Grades: Ru ≥31.9%. CAS No. 34513-98-9. Molecular formula: Ru(NO)(NO3)x(OH)y, x+y=3. Mole weight: 318.10. Symbol: GHS05. Safty Description: Danger. Hazard statements: H314. | |
(R)-(+)-XylBINAP Quick inquiry Where to buy Suppliers range | (R)-(+)-XylBINAP. Uses: Ligand used in copper-catalyzed asymmetric Mannich-type reactions of N-acylimino esters. Ligand used in the enantioselective fluorination of oxindoles. Ligand used in [2+2+2] cycloaddition of tetraynes and hexaynes. Ligand used in the asymmetric reduction of ketone via ruthenium-catalyzed transfer hydrogenation. Asymmetric hydroboration of unsaturated imines. Group: Heterocyclic Organic Compound. CAS No. 137219-86-4. Molecular formula: C52H48P2. Mole weight: 734.904g/mol. IUPAC Name: [1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane. Rotatable Bond Count: 7. Exact Mass: 734.323g/mol. SMILES: CC1=CC (=CC (=C1)P (C2=C (C3=CC=CC=C3C=C2)C4=C (C=CC5=CC=CC=C54)P (C6=CC (=CC (=C6)C)C)C7=CC (=CC (=C7)C)C)C8=CC (=CC (=C8)C)C)C. InChI: InChI=1S/C52H48P2/c1-33-21-34(2)26-43(25-33)53(44-27-35(3)22-36(4)28-44)49-19-17-41-13-9-11-15-47(41)51(49)52-48-16-12-10-14-42(48)18-20-50(52)54(45-29-37(5)23-38(6)30-45)46-31-39(7)24-40(8)32-46/h9-32H,1-8H3. InChIKey: MXGXXBYVDMVJAO-UHFFFAOYSA-N. Monoisotopic Mass: 734.323g/mol. | |
[(S)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II) Dichloride Quick inquiry Where to buy Suppliers range | [(S)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II) Dichloride. Uses: Enantioselective catalyst for the asymmetric hydrogenation of α,β-unsaturated olefins. Efficient catalyst for the asymmetric reduction of carbonyl groups, such as β-ketoesters. Group: Ruthenium series catalysts. Alternative Names: (R)-[2,2 inverted exclamation marka-Bis(diphenylphosphino)-1,1 inverted exclamation marka-binaphthyl]dichlororuthenium; C44H34Cl2P2Ru; DICHLORO[(R)-(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-; KS-00000HO2; Dichloro [(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphathyl] ruthenium(II); [R-(R*, R*)]-7-[2-(4-Fluorophenyl)-5-(1-methylethyl)-3-phenyl-4-(phenylaminocarbonyl)-1H-pyrrol-1-yl]-3,5-dihydroxy-heptanoic acid calcium salt; (R)-[1,1 inverted exclamation marka-Binaphthalene]-2,2 inverted exclamation marka-diylbis[diphenylphosphine]ruthenium complex; 134524-84-8; ST24030314; [(R)-[1,1 inverted exclamation marka-Binaphthalene]-2,2 inverted exclamation marka-diylbis[diphenylphosphine-|EP]]dichloro-ruthenium. CAS No. 134524-84-8. Molecular formula: C44H32Cl2P2Ru. Mole weight: 794.658g/mol. IUPAC Name: dichlororuthenium;[1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Rotatable Bond Count: 7. Exact Mass: 794.04g/mol. SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=CC=C7)C8=CC=CC=C8. Cl[Ru]Cl. InChI: InChI=1S/C44H32P2.2ClH.Ru/c1-5-19-35(20-6-1)45(36-21-7-2-8-22-36)41-31-29-33-17-13-15-27-39(33)43(41)44-40-28-16-14-18-34(40)30-32-42(44)46(37-23-9-3-10-24-37)38-25-11-4-12-26-38;;;/h1-32H;2*1H;/q;;;+2/p-2. InChIKey: YEKBVMDAGDTOQB-UHFFFAOYSA-L. Monoisotopic Mass: 794.04g/mol. | |
(S)-(-)-XylBINAP Quick inquiry Where to buy Suppliers range | (S)-(-)-XylBINAP. Uses: Ligand used in copper-catalyzed asymmetric Mannich-type reactions of N-acylimino esters. Ligand used in the enantioselective fluorination of oxindoles. Ligand used in [2+2+2] cycloaddition of tetraynes and hexaynes. Ligand used in the asymmetric reduction of ketone via ruthenium-catalyzed transfer hydrogenation. Asymmetric hydroboration of unsaturated imines. Group: Heterocyclic Organic Compound. CAS No. 135139-00-3. Molecular formula: C52H48P2. Mole weight: 734.904g/mol. IUPAC Name: [1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane. Rotatable Bond Count: 7. Exact Mass: 734.323g/mol. SMILES: CC1=CC (=CC (=C1)P (C2=C (C3=CC=CC=C3C=C2)C4=C (C=CC5=CC=CC=C54)P (C6=CC (=CC (=C6)C)C)C7=CC (=CC (=C7)C)C)C8=CC (=CC (=C8)C)C)C. InChI: InChI=1S/C52H48P2/c1-33-21-34(2)26-43(25-33)53(44-27-35(3)22-36(4)28-44)49-19-17-41-13-9-11-15-47(41)51(49)52-48-16-12-10-14-42(48)18-20-50(52)54(45-29-37(5)23-38(6)30-45)46-31-39(7)24-40(8)32-46/h9-32H,1-8H3. InChIKey: MXGXXBYVDMVJAO-UHFFFAOYSA-N. Monoisotopic Mass: 734.323g/mol. | |
Tetrakis (triphenylphosphine)palladium, Pd : 9.2 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·For elimination reaction, reduction reaction and alkylation reaction; ·Make alkenyl chloride and alkyl lithium or Grignard reagent generate alkene and maintain configuration; ·Make alkenyl chloride and potassium cyanide generate alkenyl cyanide; ·Synthesis of ketones from acid chlorides; deodorization of brominated ketones with hydrogen; ·Preparation of alkynes and enones; ·Cyclization of rings in asymmetric biphenyls; ·Isomerization of diene epoxides, allyl acetate; ·Stereosynthesis of alkenes and 1,4-dienes; ·Dimerization of butadiene. Group: Colloidal Catalysts. CAS No. 14221-01-3. Molecular Weight: 1155.56 g/mol. SMILES: [Pd]. c1ccc (cc1)P (c2ccccc2)c3ccccc3. c4ccc (cc4)P (c5ccccc5)c6ccccc6. c7ccc (cc7)P (c8ccccc8)c9ccccc9. c%10ccc (cc%10)P (c%11ccccc%11)c%12ccccc%12. InChI: NFHFRUOZVGFOOS-UHFFFAOYSA-N. Boiling Point: 103-107 °C. Flash Point: 99 %. Density: Soluble in benzene, toluene, insoluble in ether and alcohol. | |
triphenylphosphine rhodium chloride Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·Efficient hydrogenation catalyst and complexing agent; ·Selective hydrogenation, transfer hydrogenation; ·Hydrogenation and hydroformylation of alkenes and alkynes; ·Cyclization of 4-alkenals; ·Reductive decarbonylation of aldehydes; desulphurization of xanthyl halides; ·Reduction of diazofluoroborate; ·Hydrosilylation of carbonyl groups; ·Splitting of allyl ethers, etc. Group: Colloidal Catalysts. CAS No. 14694-95-2. Molecular Weight: 925.22 g/mol. SMILES: Cl[Rh]. c1ccc(cc1)P(c2ccccc2)c3ccccc3. c4ccc(cc4)P(c5ccccc5)c6ccccc6. c7ccc(cc7)P(c8ccccc8)c9ccccc9. InChI: IXAYKDDZKIZSPV-UHFFFAOYSA-M. Boiling Point: 245-250 °C (dec.). Flash Point: 97 %. Density: Soluble in most solvents (e.g. benzene, ethanol, chloroform, dichloromethane) but with phosphine dissociation. Reacts with O{2} in solution. | |
Tris(2,2'-bipyridine)ruthenium dichloride Quick inquiry Where to buy Suppliers range | Tris(2,2'-bipyridine)ruthenium dichloride. Group: Ruthenium Complexes. Alternative Names: 2,2''-Bipyridyl ruthenous dichloride. Grades: 99%. CAS No. 14323-06-9. Product ID: ACM14323069-3. Molecular formula: C30H24Cl2N6Ru. Mole weight: 640.53. IUPAC Name: Dichlororuthenium;2-pyridin-2-ylpyridine. Appearance: Bright red crystalline powder. SMILES: C1=CC=NC(=C1)C2=CC=CC=N2. C1=CC=NC(=C1)C2=CC=CC=N2. C1=CC=NC(=C1)C2=CC=CC=N2. Cl[Ru]Cl. | |
Tris[4,4'-bis(t-butyl)-2,2'-bipyridine]ruthenium(II) hexafluorophosphate Quick inquiry Where to buy Suppliers range | Tris[4,4'-bis(t-butyl)-2,2'-bipyridine]ruthenium(II) hexafluorophosphate. Group: Ruthenium Complexes. Alternative Names: Ru(dtbpy)3(PF6)2. Grades: 95%. CAS No. 75777-87-6. Product ID: ACM75777876-3. Molecular formula: C54H72F12N6RuP2. Mole weight: 1196.2. Appearance: Red powder. SMILES: CC (C) (C)C1=CC (=NC=C1)C2=NC=CC (=C2)C (C) (C)C. CC (C) (C)C1=CC (=NC=C1)C2=NC=CC (=C2)C (C) (C)C. CC (C) (C)C1=CC (=NC=C1)C2=NC=CC (=C2)C (C) (C)C. F[P-] (F) (F) (F) (F)F. F[P-] (F) (F) (F) (F)F. [Ru+3]. |