Nickel Carbonate Suppliers USA
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Product | Description | |
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Nickel carbonate Quick inquiry Where to buy Suppliers range | Nickel carbonate. Group: Heterocyclic Organic Compound. Alternative Names: NICKEL HYDROXIDE CARBONATE;NICKEL CARBONATE (OUS);NICKEL CARBONATE;NICKEL(II) CARBONATE;NICKELOUS CARBONATE;c.i.77779;carbonicacid, nickel(2+)salt;Carbonicacid, nickel(2+)salt(1:1). CAS No. 3333-67-3. Molecular formula: CNiO3. Mole weight: 118.7. Symbol: GHS07,GHS08,GHS09. Safty Description: 22-36/37-60-61. Hazard statements: Xn, N. Supplemental Hazard Statements: H302-H315-H317-H332-H334-H341-H350-H360-H372-H400-H410. | |
Nickel carbonate Quick inquiry Where to buy Suppliers range | Nickel carbonate. CAS No. 958638-02-3. Pack Sizes: 20kg. Product ID: NL-NC-01. Categories: nickel(ii) carbonate, nickelous carbonate, nickel monocarbonate, carbonic acid. | |
Nickel carbonate, basic hydrate Quick inquiry Where to buy Suppliers range | Nickel carbonate, basic hydrate. CAS No. 958638-02-3. Molecular formula: NiCO3 · 2Ni(OH)2 · xH2O. Mole weight: 304.12 (anhydrous basis). | |
Nickel carbonate hydroxide teteahydrate Quick inquiry Where to buy Suppliers range | Nickel carbonate hydroxide teteahydrate. Group: Nickel Complexes. Alternative Names: Nickel(II) carbonate basic tetrahydrate. Grades: 98%. CAS No. 12244-51-8. Product ID: ACM12244518-1. Molecular formula: C2H20Ni5O16. Mole weight: 593.64. Appearance: Powder. SMILES: C(=O)([O-])[O-]. C(=O)([O-])[O-]. O. O. O. O. O. O. O. O. O. O. [Ni]. [Ni]. [Ni]. [Ni+2]. [Ni+2]. | |
Nickel Carbon Core Shell Nanoparticles Quick inquiry Where to buy Suppliers range | Nickel Carbon Core Shell Nanoparticles. Grades: 99.9%. Product ID: ACMA00020069. | |
Nickel Carbon Nanotube Quick inquiry Where to buy Suppliers range | Nickel Carbon Nanotubes are generally immediately available in most volumes. Additional technical, research and safety (MSDS) information is available. Carbon Nanotubes are Single-Walled, Double Walled and Multi-Walled black nano scale cylindrical tubes of graphitic carbon with numerous applications. Carbon Nanotubes are the stiffest and strongest known fibers and have unique electrical properties. When used as reinforcement fibers, carbon nanotubes can improve the quality and properties of metal, polymer and ceramics. Applications for AE Carbon Nanotubes include in flat screen displays, scanning probe microscopes in brushes for commercial electric motors, and in sensing devices and because of their strength in numerous aerospace and automotive uses, in body armor and tear-resistant cloth fibers and textiles and stronger and lighter sports equipment. Carbon nanotubes can behave like a conductive metallic or semiconductor depending on their structure, which is useful for nanoscale electronic devices and in electrically conductive films in coatings, plastics, nanowire, nanofiber and in certain bioscience applications. Recently, carbon nanotubes have been demonstrated to create the "darkest" known material absorbing all wavelengths or "colors" of light which will prove useful in solar and electronic applications. When combined with Aluminum, Copper, Magnesium, Nickel, Titanium, and Tin, Single-Walled Carbon Nanotube materials reveal enhanced tensile strength, hardness and elastic modulus characteristics. Titanium/Carbon Nanotube composites, research shows demonstrate a considerable increase in tensile stress, hardness and yield stress. In an additional study, when compared to pure Titanium, Titanium/Carbon Nanotube composites displayed increased property hardness of the metal as well as improved elastic modulus. Group: Carbon. Product ID: ACMA00024298. Molecular formula: SiC. Appearance: Powder. | |
Nickel Carbon Nanotubes Quick inquiry Where to buy Suppliers range | Nickel Carbon Nanotubes. Product ID: ACMA00000291. Molecular formula: SiC. Appearance: Powder. | |
Nickel Carbon-Coated nanoparticles Quick inquiry Where to buy Suppliers range | Nickel Carbon-Coated nanoparticles. Product ID: ACMA00019684. | |
Nickel (II) Carbonate Quick inquiry Where to buy Suppliers range | NICKEL (II) CARBONATE, 99.9% pure, -100 mesh, (Synonym: Nickelous Carbonate), Formula: NiCO3. CAS No. 3333-67-3. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
Nickel(II) carbonate basic hydrate Quick inquiry Where to buy Suppliers range | Nickel(II) carbonate basic hydrate. Uses: NICKEL(II) CARBONATE BASIC HYDRATE is used in some ceramic applications and as precursors to catalysts. Group: Metal & Ceramic Materials. Alternative Names: NICKEL(II) HYDROXIDE CARBONATE HYDRATE;NICKEL(II) CARBONATE TETRAHYDRATE;NICKEL CARBONATE, BASIC;NICKEL CARBONATE, BASIC HYDRATE;NICKEL(II) CARBONATE BASIC HYDRATE;(carbonato(2-))tetrahydroxytri-nicke;[carbonato(2-)]tetrahydroxytri-nicke;[carbonato(2-)]te. CAS No. 12607-70-4. Molecular formula: ~NiCO3 · 2Ni(OH)2 · 4H2O. Mole weight: 322.13. | |
Nickel(ii)carbonate basic tetrahydrate Quick inquiry Where to buy Suppliers range | Light green powder. Group: Electrolytes. Alternative Names: NICKEL(II) CARBONATE BASIC TETRAHYDRATE;NICKELOUS CARBONATE, BASIC, TETRAHYDRATE;NICKEL(II) CARBONATE HYDROXIDE TETRAHYDRATE;Nickel(?) carbonate hydroxide tetrahydrate;Nickel carbonate hydroxide (Ni5(CO3)2(OH)6), tetrahydrate. CAS No. 12244-51-8. IUPAC Name: nickel; nickel(2+); dicarbonate; decahydrate. Molecular Weight: 587.59. Molecular Formula: C2H14Ni5O16. SMILES: C(=O)([O-])[O-]. C(=O)([O-])[O-]. O. O. O. O. O. O. O. O. O. O. [Ni]. [Ni]. [Ni]. [Ni+2]. [Ni+2]. InChIKey: KSQJQIDWVHEXCI-UHFFFAOYSA-J. Purity: 96%. Density: 2.6. | |
Nickel(II) carbonate basic tetrahydrate 98+% (48-50% ex Ni). Quick inquiry Where to buy Suppliers range | Nickel(II) carbonate basic tetrahydrate 98+% (48-50% ex Ni). Group: Biochemicals. Grades: Highly Purified. CAS No. 12607-70-4. Pack Sizes: 100g, 250g, 25g, 1Kg, 2.5Kg. US Biological Life Sciences. | Worldwide |
Nickel Nanoparticles, Carbon Coated Quick inquiry Where to buy Suppliers range | Nickel Nanoparticles, Carbon Coated. Grades: 99.9 %. Product ID: ACMA00019591. | |
MWCNT-Ni Type 1 Carbon Nanotubes Multi Walled, Nickel coated Quick inquiry Where to buy Suppliers range | MWCNT-Ni Type 1 Carbon Nanotubes Multi Walled, Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
MWCNT-Ni Type 2 Carbon Nanotubes Multi Walled , Nickel coated Quick inquiry Where to buy Suppliers range | MWCNT-Ni Type 2 Carbon Nanotubes Multi Walled , Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
MWCNT-Ni Type 3 Carbon Nanotubes Multi Walled , Nickel coated Quick inquiry Where to buy Suppliers range | MWCNT-Ni Type 3 Carbon Nanotubes Multi Walled , Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
MWCNT-Ni Type 4 Carbon Nanotubes Multi Walled , Nickel coated Quick inquiry Where to buy Suppliers range | MWCNT-Ni Type 4 Carbon Nanotubes Multi Walled , Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
Nickel-Coated Multi Walled Carbon Nano Tubes Quick inquiry Where to buy Suppliers range | Nickel-Coated Multi Walled Carbon Nano Tubes. Product ID: ACMA00020390. | |
Nickel Coated Multi-walled Carbon Nanotubes Quick inquiry Where to buy Suppliers range | Nickel Coated Multi-walled Carbon Nanotubes. Product ID: ACMA00020389. | |
High-temperature steel with 24,4% chromium, 19,7% nickel, 2% silicon and 0,15% carbon-chips Quick inquiry Where to buy Suppliers range | High-temperature steel with 24,4% chromium, 19,7% nickel, 2% silicon and 0,15% carbon-chips. Uses: For analytical and research use. Group: Metal alloys. Catalog: APS008762. Shipping: Room Temperature. | |
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. | |
2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl Quick inquiry Where to buy Suppliers range | 2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl. Uses: Phosphine Ligand Kit component. Useful ligand for palladium-catalyzed carbon-nitrogen bond formation. Useful ligand for rhodium-catalyzed C-C bond formation. Useful ligand for palladium-catalyzed intramolecular acylation of aryl bromides via C-H activation. Used in the preparation of Buchwald third generation precatalyst. Used in methoxy directed Rhodium migration. Used in Nickel catalyzed C-N cross-coupling reactions. Group: Organic Phosphine Compounds. Alternative Names: F0001-2326; DB-009478; AC1LCPMX; (S)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL; AN-10356; SC-19338; (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene, puriss.; PubChem8136; TL8005203; (S)-(-)-2,2 inverted exclamation mark -Bis(diphenylphosphino)-1,1 inverted exclamation mark -binaphthalene. CAS No. 98327-87-8. Molecular formula: C44H32P2. Mole weight: 622.688g/mol. IUPAC Name: [1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Rotatable Bond Count: 7. Exact Mass: 622.198g/mol. EC Number: 616-304-7. 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. InChI: InChI=1S/C44H32P2/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. InChIKey: MUALRAIOVNYAIW-UHFFFAOYSA-N. Monoisotopic Mass: 622.198g/mol. | |
4,4'-Di-tert-butyl-2,2'-bipyridine Quick inquiry Where to buy Suppliers range | 4,4'-Di-tert-butyl-2,2'-bipyridine. Uses: Ligand for the iridium-catalyzed borylation of arenes Ligand for the iridium-catalyzed synthesis of arylboronic acids and aryl trifluoroborates Ligand for the nickel-catalyzed hydroxycarboxylation of 1,2-dienes by reaction carbon dioxide and oxygen Ligand for the iridium-catalyzed meta borylation followed by halogenation of 1,3-disubstituted arenes Ligand for the iridium-catalyzed silyl-directed ortho-borylation of arenes Ligand for the iridium-catalyzed silane borylation followed by aryl borylation Ligand for the iridium-catalyzed microwave-accelerated borylation of aromatic C-H bonds Ligand for the iridium-catalyzed silyl-directed borylation of indoles Ligand for the nickel-catalyzed synthesis of functionalized dialkyl ketones from carboxylic acids and alkyl halides Ligand for the iron-catalyzed arylation of heterocycles. Group: Polymer/Macromolecule. CAS No. 72914-19-3. Molecular formula: C18H24N2. Mole weight: 268.404g/mol. IUPAC Name: 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine. Rotatable Bond Count: 3. Exact Mass: 268.194g/mol. SMILES: CC (C) (C)C1=CC (=NC=C1)C2=NC=CC (=C2)C (C) (C)C. InChI: InChI=1S/C18H24N2/c1-17(2,3)13-7-9-19-15(11-13)16-12-14(8-10-20-16)18(4,5)6/h7-12H,1-6H3. InChIKey: TXNLQUKVUJITMX-UHFFFAOYSA-N. H-Bond Acceptor: 2. Monoisotopic Mass: 268.194g/mol. | |
Bis(triphenylphosphine)nickel dicarbonyl Quick inquiry Where to buy Suppliers range | Bis(triphenylphosphine)nickel dicarbonyl. Group: Nickel Complexes. Alternative Names: Carbon monoxide;nickel;triphenylphosphane. Grades: 98%. CAS No. 13007-90-4. Product ID: ACM13007904. Molecular formula: C38H30NiO2P2. Mole weight: 639.29. Appearance: Crystal. SMILES: [C-]#[O+]. [C-]#[O+]. 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. [Ni]. | |
Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- [bis (4-fluorophenyl] phosphino] ferrocenyl] ethyldi-tert-butylphosphine] nickel (II) Quick inquiry Where to buy Suppliers range | Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- [bis (4-fluorophenyl] phosphino] ferrocenyl] ethyldi-tert-butylphosphine] nickel (II). Uses: 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. CAS No. 2049086-37-3. Mole weight: 774.69. | |
Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldicyclohexylphosphine] nickel (II) Quick inquiry Where to buy Suppliers range | Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldicyclohexylphosphine] nickel (II). Uses: 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. CAS No. 2049086-35-1. Mole weight: 802.88. | |
Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldiphenylphosphine] nickel (II) Quick inquiry Where to buy Suppliers range | Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldiphenylphosphine] nickel (II). Uses: 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. CAS No. 2049086-36-2. Mole weight: 790.79. | |
Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II) Quick inquiry Where to buy Suppliers range | Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II). Uses: 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. CAS No. 2049086-34-0. Mole weight: 738.71. | |
Fluopsin N Quick inquiry Where to buy Suppliers range | Fluopsin N is an antibiotic containing metallic nickel produced by Pseudomonas fluorescent KY 4032 cultured with n-alkane as a carbon source. It has strong anti-Gram-positive and negative bacteria activity and anti-tumor activity. CAS No. 31541-90-9. Molecular formula: C4H8O2N2S2Ni. Mole weight: 238.94. | |
Graphene Dispersion in Water (Dia:1-3μm) Quick inquiry Where to buy Suppliers range | Carbon black oil appears as a dark colored liquid with a petroleum-like odor. Less dense than water and insoluble in water. Vapors heavier than air.;Carbon, activated is a black grains that have been treated to improve absorptive ability. May heat spontaneously if not properly cooled after manufacture.;Carbon, animal or vegetable origin appears as a black powder or granular mixed with a tar or starch and water binder pressed into regular lumps or briquettes. Heats slowly and ignites in air especially if wet.;Graphite (natural) appears as a mineral form of the element carbon. Hexagonal crystals or thin leaf-like layers. Steel-gray to black with a metallic luster and a greasy feel. An electrical conductor. Used for high-temperature crucibles, as a lubricant and in "lead" pencils.;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, WetSolid, OtherSolid, Liquid; DryPowder, WetSolid, Liquid; Liquid; OtherSolid; OtherSolid, GasVapor, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid, Liquid; WetSolid; WetSolid, Liquid;OtherSolid; PelletsLargeCrystals;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;Black, odourless powder;BLACK POWDER OR SOLID IN VARIOUS FORMS. ODOURLESS WHEN PURE.;BLACK FLAKES, LUMPS, POWDER OR CHIPS.;ODOURLESS BLACK PELLETS OR EXTREMELY FINE POWDER.;Black, odorless solid or a dark colored liquid with a petroleum-like odor.;Black grains that have been treated to improve absorptive ability.;Steel gray to black, greasy feeling, odorless solid;Black, odorless solid.;Steel gray to black, greasy feeling, odorless solid.;Steel gray to black, greasy feeling, odorless solid. Uses: ?Lithium ion and nickel-hydrogen battery-as high conductive components in battery slurry. ?Supercapacitor -conductive reagents of the supercapacitor electrodes. ?Lead acid cell, solar cell and semiconductor industry. ?Other conductive industry. Group: Other Nanomaterials. CAS No. 7782-42-5. IUPAC Name: carbon. Molecular Weight: C;C. Molecular Formula: 12.011g/m | |
Mechanically Exfoliated Monolayer WSe2 On Substrates Quick inquiry Where to buy Suppliers range | Multi walled carbon nanotubes (MWNTs, CNTs) was prepared by plasma enhanced chemical vapor deposition (PECVD). The CNTs formed can be formed in bundles over a catalyst support or in patterns over substrates.1 Each MWCNT is tipped with nickel-catalyst particle with diameter equal to diameter of the nanotube. Uses: An excellent device material for studying the number of layers and fluorescence effects. CAS No. 12067-46-8 (WSe2); 60676-86-0 (SiO2). Product ID: ACM12067468-3. | |
[N-[1-[2- (2-Pyridylcarboxamido) phenyl]ethylidene]glycinato]nickel Quick inquiry Where to buy Suppliers range | [N-[1-[2- (2-Pyridylcarboxamido) phenyl]ethylidene]glycinato]nickel. Group: Heterocyclic Organic Compound. CAS No. 264921-97-3. Molecular formula: C16H14N3NiO3-. Mole weight: 354.999g/mol. IUPAC Name: [2-[N-(carboxymethyl)-C-methylcarbonimidoyl]phenyl]-(pyridine-2-carbonyl)azanide;nickel. Rotatable Bond Count: 1. Exact Mass: 354.039g/mol. SMILES: CC(=NCC(=O)O)C1=CC=CC=C1[N-]C(=O)C2=CC=CC=N2.[Ni]. InChI: InChI=1S/C16H15N3O3.Ni/c1-11(18-10-15(20)21)12-6-2-3-7-13(12)19-16(22)14-8-4-5-9-17-14;/h2-9H,10H2,1H3,(H2,18,19,20,21,22);/p-1. InChIKey: FWLGSJHKMDCFKF-UHFFFAOYSA-M. H-Bond Donor: 1. H-Bond Acceptor: 6. Monoisotopic Mass: 354.039g/mol. | |
N6-Carbobenzyloxy-N2,N2-bis(carboxymethyl)-L-lysine Quick inquiry Where to buy Suppliers range | It is used in the synthesis of nickel-chelating fluorinated lipids for protein monolayer crystallizations. Group: Biochemicals. Alternative Names: N2, N2-Bis (carboxymethyl) -N6-[ (phenylmethoxy) carbonyl]-. Grades: Highly Purified. CAS No. 113231-04-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
Nickel(II) acetylacetonate, 96% Quick inquiry Where to buy Suppliers range | Nickel(II) acetylacetonate, 96%. Group: General Materials & Solvents. Alternative Names: Carbonic acid dicesium. CAS No. 3264-82-2. Molecular Weight: C10H14NiO4. Molecular Formula: 257. Purity: 96%. | |
[N-[Phenyl[2-[[[(1S, 2R)-1-(phenylmethyl)-2-pyrrolidinyl-κ N]carbonyl]amino-κ N]phenyl]methylene]glycinato(2-)-κ N, κ O]nickel Quick inquiry Where to buy Suppliers range | [N-[Phenyl[2-[[[(1S, 2R)-1-(phenylmethyl)-2-pyrrolidinyl-κ N]carbonyl]amino-κ N]phenyl]methylene]glycinato(2-)-κ N, κ O]nickel. Group: Nickel Complexes. Alternative Names: (R)-2-{o-{(N-Benzylprolyl)amino}phenyl}-benzylideneamino-acetato(2-)-N,N',N''-nickel(II). Grades: 98%. CAS No. 172924-51-5. Product ID: ACM172924515. Molecular formula: C27H25N3NiO3. Mole weight: 498.2. SMILES: C1CC (N (C1)CC2=CC=CC=C2)C (=NC3=CC=CC=C3C (=NCC (=O)[O-])C4=CC=CC=C4)[O-]. [Ni]. | |
(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 | |
(SP-4-4)-[N-[[5-Chloro-2-[[[(1S, 2R)-1-(phenylmethyl)-2-pyrrolidinyl-κ N]carbonyl]amino-κ N]phenyl]phenylmethylene]glycinato(2-)-κ N, κ O]-nickel Quick inquiry Where to buy Suppliers range | (SP-4-4)-[N-[[5-Chloro-2-[[[(1S, 2R)-1-(phenylmethyl)-2-pyrrolidinyl-κ N]carbonyl]amino-κ N]phenyl]phenylmethylene]glycinato(2-)-κ N, κ O]-nickel. Group: Nickel Complexes. Alternative Names: 2-[[[2-[(2R)-1-Benzylpyrrolidine-2-carbonyl]azanidyl-5-chlorophenyl]-phenylmethylidene]amino]acetate; nickel(3+). Grades: 98%. CAS No. 1021603-69-9. Product ID: ACM1021603699. Molecular formula: C27H24ClN3NiO3. Mole weight: 532.64. SMILES: C1CC(N(C1)CC2=CC=CC=C2)C(=O)[N-]C3=C(C=C(C=C3)Cl)C(=NCC(=O)[O-])C4=CC=CC=C4.[Ni+3]. |