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3-BROMOBENZYLZINC BROMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

307496-31-7

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307496-31-7 Usage

Uses

It is employed as a intermediate for pharmaceutical.

Check Digit Verification of cas no

The CAS Registry Mumber 307496-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,7,4,9 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 307496-31:
(8*3)+(7*0)+(6*7)+(5*4)+(4*9)+(3*6)+(2*3)+(1*1)=147
147 % 10 = 7
So 307496-31-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Br.BrH.Zn/c1-6-3-2-4-7(8)5-6;;/h2-5H,1H2;1H;/q;;+1/p-1/rC7H6Br2Zn/c8-7-3-1-2-6(4-7)5-10-9/h1-4H,5H2

307496-31-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H58983)  3-Bromobenzylzinc bromide, 0.5M in THF, packaged under Argon in resealable ChemSeal? bottles   

  • 307496-31-7

  • 50ml

  • 1702.0CNY

  • Detail

307496-31-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-BROMOBENZYLZINC BROMIDE

1.2 Other means of identification

Product number -
Other names 3-bromobenzylzinc bromide solution

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:307496-31-7 SDS

307496-31-7Relevant academic research and scientific papers

The synthesis of 1,2-diarylindenes via DDQ-mediated dehydrogenative intramolecular cyclization

Li, Yi,Cao, Li,Luo, Xiaoyan,Deng, Wei-Ping

, p. 5974 - 5979 (2014)

A direct DDQ-mediated dehydrogenative intramolecular cyclization of (Z)-1,2,3-triaryl substituted propylenes promoted by Cu(OAc)2 was developed, providing 1,2-diarylindene derivatives in moderate to good yields (up to 92%) under mild conditions

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