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

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

• 245416-52-8 4-benzyl-2,5-di-tert-butyl-6-hydroxycyclohexa-2,5-dien-1-one 
• 162977-46-0 di-μ-tert-butylimido-bis[benzyl(tert-butylimido)manganese(V)] 
• 197807-43-5 Zn(CH₂Ph)2(N,N,N',N'-tetramethylethylenediamine) 
• 1291093-04-3 [Re(κ1(P)-6-(diphenylphosphino)-2,2'-bipyridine*ZnBn)(CO)4(COBn)][OTf] 
• 59326-12-4 Ta(CH₂C₆H₅)Cl₄ 
• 108-88-3 toluene 
• 74920-39-1 TaCl₃(CH₂Ph)2 
• 59326-13-5 Cl₂Ta(CH₂Ph)3 
• 245416-53-9 4-benzyl-3,6-di-tert-butyl-1,2-benzoquinone 
• 1485-70-7 N-benzylbenzamide 
• 620-40-6 tribenzylamine 

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.

Cycloaddition and C-H Activation Reactions of a Tantalum Alkylidyne

The alkylidyne complex (C5Me5)Ta(≡CPh)-(PMe3)2Cl (1) was first reported by Schrock in 1978, but little if any follow-up work on 1 or other group 5 metal alkylidynes has been reported. This work discloses two ave

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.

Heterobimetallic complexes of rhenium and zinc: Potential catalysts for homogeneous syngas conversion

6-(Diphenylphosphino)-2,2′-bipyridine (PNN) coordinates to rhenium carbonyls in both κ1(P) and κ2(N,N) modes; in the former, the free bpy moiety readily binds to zinc alkyls and halides. [Re(κ1(P)-PNN)(CO)5][OTf

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

SYNTHESE ORGANOMETALLIQUE D'α-AMINOESTERS N,N-DISUBSTITUES

Reaction of organozinc compounds with a particular gem-aminoether ester, i.e. methyl-N,N-diethylamino methoxyacetate, leads to α-aminoesters.This method allows the synthesis of compounds having potential biological activity, viz. β-unsaturated α-aminoesters.