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820963-51-7

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820963-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 820963-51-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,0,9,6 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 820963-51:
(8*8)+(7*2)+(6*0)+(5*9)+(4*6)+(3*3)+(2*5)+(1*1)=167
167 % 10 = 7
So 820963-51-7 is a valid CAS Registry Number.

820963-51-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[tert-butyl(diphenyl)silyl]oxy-2-methylpropanoic acid

1.2 Other means of identification

Product number -
Other names Propanoic acid,3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-methyl

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:820963-51-7 SDS

820963-51-7Relevant articles and documents

New Strategy for Forging Contiguous Quaternary Carbon Centers via H 2 O 2 -Mediated Ring Contraction

Hu, Jiadong,Yu, Xin,Xie, Weiqing

, p. 2517 - 2524 (2017/09/28)

Stereospecific construction of contiguous quaternary carbon centers constitutes a major challenge in natural product synthesis. A general protocol that enables stereospecific construction of all stereoisomers of such a moiety remains elusive. In this article, we will discuss the oxidative ring contraction of all-substituted cyclic α-formyl ketones mediated by H 2 O 2, which provides a facile access to the stereospecific construction of contiguous quaternary carbon centers.

Intramolecular Amidoalkylation of Chiral Iminium Ions: Stereoselective Synthesis of syn-1,3-Aminoalcohols

Hioki, Hideaki,Okuda, Manabu,Miyagi, Waka,Ito, Sho

, p. 6131 - 6134 (2007/10/02)

The intramolecular Hosomi-Sakurai reaction of 3-siloxybutaniminium salts exhibited a syn selectivity of up to 51:1, while the same type of reaction of 2-methyl-3-siloxypropaniminium salts showed up to 290:1 syn selectivity.

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