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147331-83-7

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147331-83-7 Usage

General Description

2H-1,3-Thiazine-4-carboxylic acid, tetrahydro-, (4S)-(9CI) is a chemical compound with the molecular formula C5H7NO2S. It is a derivative of thiazine and carboxylic acid with a tetrahydro structure. 2H-1,3-Thiazine-4-carboxylicacid,tetrahydro-,(4S)-(9CI) is a chiral molecule with a specific stereochemistry, denoted by the designation (4S)-(9CI). The compound has potential applications in pharmaceuticals and organic synthesis due to its unique structure and properties, and it may be used in the development of new drugs or as a building block in chemical reactions. Its precise applications and properties would depend on further research and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 147331-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,3,3 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 147331-83:
(8*1)+(7*4)+(6*7)+(5*3)+(4*3)+(3*1)+(2*8)+(1*3)=127
127 % 10 = 7
So 147331-83-7 is a valid CAS Registry Number.

147331-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2H-1,3-Thiazine-4-carboxylicacid,tetrahydro-,(4S)-(9CI)

1.2 Other means of identification

Product number -
Other names L-tert-leucine HCl salt

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:147331-83-7 SDS

147331-83-7Downstream Products

147331-83-7Relevant articles and documents

Preparations of Optically Active Homocysteine and Homocystine by Asymmetric Transformation of (RS)-1,3-Thiazane-4-carboxylic Acid

Miyazaki, Hideya,Ohta, Atsushi,Kawakatsu, Nobuyuki,Waki, Yukitaka,Gogun, Yasuhiro,et al.

, p. 536 - 540 (2007/10/02)

DL-Homocysteine from (RS)-homocysteine thiolactone hydrochloride was subjected to reaction with formaldehyde in acetic acid to give (RS)-1,3-thiazane-4-carboxylic acid monohydrate .An asymmetric transformation of (RS)-THA*H2O was achieved via salt formation with optically active tartaric acid in the presence of salicylaldehyde in acetic acid.The (R)- and (S)-THA obtained, respectively, from the salt of (R)-THA with (2R,3R)-tartaric acid and its enantiomeric salt were treated with hydroxylamine hydrochloride to give D- and L-Hcy of 100percent optical purity, respectively, in 50percent yield from (RS)-HTL*HCl.Oxidation of D- and L-Hcy with hydrogen peroxide gave D- and L-homocystine, respectively, in 47percent yield.

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