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NICKEL (II) CHLORIDE, ANHYDROUS, 99.99% pure, -10 mesh, (Synonym: Nickelous Chloride), Formula: NiCl2. CAS No. 7718-54-9. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
Texas TX
Nickel (II) Chloride
Nickel (II) Chloride. Grades: 99.95% Extremely High (>=99%). CAS No. 7791-20-0. Pack Sizes: Gram Quantities: 250 gm, 1 kg. Order Number: 2683.
www.prochemonline.com
Nickel (II) Chloride
NICKEL (II) CHLORIDE, HEXAHYDRATE, 99.5% pure, -20 mesh, (Synonym: Nickelous Chloride, Hexahydrate), Formula: NiCl2.6H2O. CAS No. 7791-20-0. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
Texas TX
Nickel (II) Chloride Hexahydrate, Reagent Grade, 100 g
Formula: NiCl2 6H2O. F. W: 237. 69. Characteristics: Green crystals or crystalline powder. Notes: Deliquescent. Storage Code: Blue; toxic. Alternative Names: Nickelous chloride hexahydrate. Grades: chem-grade reagent. CAS No. 7791-20-0. Product ID: 877142. -- SOLD FOR EDUCATIONAL USE ONLY --
Nickel (II) Chloride Hydrate, 99.95%
Nickel (II) Chloride Hydrate, 99.95%. CAS No: 69098-15-3
Sarchem Laboratories New Jersey NJ
[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.
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.
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 (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] 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.
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.
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