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153123-10-5

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153123-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153123-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,2 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 153123-10:
(8*1)+(7*5)+(6*3)+(5*1)+(4*2)+(3*3)+(2*1)+(1*0)=85
85 % 10 = 5
So 153123-10-5 is a valid CAS Registry Number.

153123-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (SS,R)-(E)-2-(p-tolylsulfinyl)-1-(trimethylsilyl)-1-octen-3-ol

1.2 Other means of identification

Product number -
Other names -

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:153123-10-5 SDS

153123-10-5Downstream Products

153123-10-5Relevant articles and documents

Preparation of optically pure propargylic and allylic alcohols from 2-(trimethylsilyl)vinyl sulfoxides as a chiral ethynyl anion synthon: Computational studies on elimination reaction of 2-(trimethylsilyl)vinyl sulfoxides

Nakamura, Shuichi,Kusuda, Shinya,Kawamura, Kiyoshi,Toru, Takeshi

, p. 640 - 647 (2007/10/03)

The reaction of the (α-carbanion derived from (trimethylsilyl)vinyl sulfoxides with aldehydes afforded a diastereomeric mixture of the products. Each diastereomer was subjected to specific elimination reactions to give optically pure propargylic, trimethylsilylated propargylic, and allylic alcohols. Acceleration of the sulfenic acid-elimination from the β-silylvinyl sulfoxide was demonstrated by the ab initio calculation to be ascribed mainly to the β-effect of the silyl group.

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