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1219805-31-8

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1219805-31-8 Usage

Uses

DL-Homocysteine Thiolactone-3,3,4,4-d4 HCl (CAS# 1219805-31-8) is a useful isotopically labeled research compound.

Check Digit Verification of cas no

The CAS Registry Mumber 1219805-31-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,8,0 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1219805-31:
(9*1)+(8*2)+(7*1)+(6*9)+(5*8)+(4*0)+(3*5)+(2*3)+(1*1)=148
148 % 10 = 8
So 1219805-31-8 is a valid CAS Registry Number.

1219805-31-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name DL-[(2)H4]homocysteine thiolactone hydrochloride

1.2 Other means of identification

Product number -
Other names DL-3-amino-4,4,5,5-tetradeutero-2-thiophenone hydrochloride

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:1219805-31-8 SDS

1219805-31-8Upstream product

1219805-31-8Relevant articles and documents

Synthesis of optically active deuterium-labeled homocysteine thiolactone

Shinohara, Yoshihiko,Hasegawa, Hiroshi,Hashimoto, Takao,Ichida, Kimiyoshi

experimental part, p. 552 - 555 (2011/04/22)

Optically pure (R)- and (S)-3-aminotetradeutero-2-thiophenone (D- and L-[2H4]homocysteine thiolactone) for use as substrates for metabolic and pharmacokinetic studies has been prepared. The racemic [ 2H4]homocysteine thiolactone hydrochloride was prepared from commercially available and highly enriched DL-[3,3,4,4-2H 4]methionine by intramolecular condensation with hydriodic acid. The racemate was derivatized with (S)-(+)-2-methoxyphenylacetic acid to form the diastereomeric amides. The diastereomers were separated by silica gel column chromatography. Hydrolysis of the D- and L-isomer amide in 4M HCl-ethanol (1:2 v/v) afforded the optically pure D- and L-[2H4] homocysteine thiolactone, respectively. Copyright

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