7029-30-3

Basic information

• Product Name: Zinc, bis(phenylmethyl)-
• CAS NO: 7029-30-3
• Molecular Formula: C14H14Zn
• Molecular Weight: 247.655
• Mol File: 7029-30-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Zinc, bis(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Zinc, bis(phenylmethyl)-(7029-30-3)
• EPA Substance Registry System: Zinc, bis(phenylmethyl)-(7029-30-3)

Safety Data

• Hazardous Substances Data: 7029-30-3(Hazardous Substances Data)

Upstream product

• 76721-55-6 Dibenzylzink-1,4-dioxan 
• 7646-85-7 zinc(II) chloride 
• 6921-34-2 benzylmagnesium chloride 
• 2785-29-7 benzyl potassium 
• 766-04-1 benzyllithium 

Downstream Products

• 10316-00-4 4-benzyl-morpholine 
• 59326-13-5 Cl₂Ta(CH₂Ph)3 
• 59326-12-4 Ta(CH₂C₆H₅)Cl₄ 
• 74920-39-1 TaCl₃(CH₂Ph)2 
• 191873-00-4 [Zn(CH₂C₆H₅)(((CH₃)3CNCH)2)]2 
• 1291093-04-3 [Re(κ1(P)-6-(diphenylphosphino)-2,2'-bipyridine*ZnBn)(CO)4(COBn)][OTf] 
• 620-40-6 tribenzylamine 
• 245416-52-8 4-benzyl-2,5-di-tert-butyl-6-hydroxycyclohexa-2,5-dien-1-one 
• 100-46-9 benzylamine 
• 61533-14-0 methyl 2-(N,N-diethylamino)-3-phenylpropanoate 

Relevant articles and documents

Remarkably Selective Formation of Allenyl and Dienyl Alcohols via Ni-Catalyzed Coupling Reaction of Conjugated Enyne, Aldehyde, and Organozinc Reagents

A nickel catalyst promotes the multi-component reactions (MCRs) of conjugated enynes, aldehydes, and organozinc reagents to form unsaturated alcohols. Ligand effects dramatically control the regioselectivity in these Ni-catalyzed MCRs, leading to the selective formation of allenyl alcohols and conjugated dienyl alcohols.

Nickel-catalyzed multicomponent coupling of alkyne, buta-1,3-diene, and dimethylzinc under carbon dioxide

A nickel catalyst promoted the coupling of alkynes with buta-1,3-diene and dimethylzinc under carbon dioxide to provide (5E,8Z)-2-vinyldeca-5,8-dienoic acids with high regio- and stereo selectivity. Georg Thieme Verlag Stuttgart. New York.

Copper-Catalyzed Electrophilic Amination of Diorganozinc Reagents

The copper-catalyzed electrophilic amination of diorganozinc reagents employing O-acyl N,N-dialkyl hydroxylamine derivatives as aminating agents is described. This reaction offers a general method for the preparation of tertiary amines in high yields and is noteworthy for its convenience both in terms of reaction conditions employed (room temperature, ≤1 h) and ease of product isolation (acid/base extractive workup). Copyright