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<3-2H2>-3-chloro-2-hydroxypropyl-p-toluenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83385-52-8

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83385-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83385-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,8 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83385-52:
(7*8)+(6*3)+(5*3)+(4*8)+(3*5)+(2*5)+(1*2)=148
148 % 10 = 8
So 83385-52-8 is a valid CAS Registry Number.

83385-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-2H2]-3-chloro-2-hydroxypropyl-p-toluenesulfonate

1.2 Other means of identification

Product number -
Other names 3-chloro-1-(tosyloxy)-2-propan-3,3-d2-ol

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:83385-52-8 SDS

83385-52-8Downstream Products

83385-52-8Relevant academic research and scientific papers

Efficient routes to isotopically labelled epichlorohydrins ((chloromethyl) oxiranes)

O'Hagan,White,Jones

, p. 871 - 880 (2007/10/02)

Efficient routes are developed for the synthesis of variously labelled 2H- and 13C- labelled epichlorohydrins prepared from appropriately labelled acetic acids and sodium borodeuteride. The route is versatile and can be used for strategic location of isotopes at C-I, C-2 and C-3 of epichlorohydrin. By way of demonstration [2-13C]-, [2-2H]-, [3-2H2] and [2-2H, 3-2H2]-epithlorohydrins have been prepared. In addition the syntheses can be adapted for the preparation of enantiomerically pure and isotopically labelled epichlorohydrins.

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