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116210-64-1

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116210-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116210-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,1 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116210-64:
(8*1)+(7*1)+(6*6)+(5*2)+(4*1)+(3*0)+(2*6)+(1*4)=81
81 % 10 = 1
So 116210-64-1 is a valid CAS Registry Number.

116210-64-1SDS

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 bis(4-bromophenyl) propanedioate

1.2 Other means of identification

Product number -
Other names Propanedioicacid,bis(4-bromophenyl) ester (9CI)

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:116210-64-1 SDS

116210-64-1Relevant articles and documents

Asymmetric catalytic 1,6-conjugate addition/aromatization of para-quinone methides: Enantioselective introduction of functionalized diarylmethine stereogenic centers

Chu, Wen-Dao,Zhang, Le-Fen,Bao, Xu,Zhao, Xian-He,Zeng, Chao,Du, Ji-Yuan,Zhang, Guo-Biao,Wang, Fang-Xin,Ma, Xiao-Yan,Fan, Chun-An

, p. 9229 - 9233 (2013)

It′s just a phase: The title reaction sequence of para-quinone methides (p-QMs) has been developed with malonates under phase-transfer catalysis. The reaction also offers an alternative route to asymmetric construction of diarylmethine stereocenters in ex

Highly enantioselective introduction of bis(alkoxycarbonyl)methyl group into the 2-position of piperidine skeleton

Matsumura, Yoshihiro,Minato, Diashirou,Onomura, Osamu

, p. 654 - 663 (2008/02/06)

Copper ion catalyzed carbon-carbon bond forming reaction of N-acyliminium ions with diaryl malonates was achieved with high enantioselectivity. The key intermediates in the method were 2-methoxy-3,4-didehydropiperidines, which were easily prepared through

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