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(5S)-5-(2-sulfanylpropan-2-yl)imidazolidine-2,4-dione is a thioimidazolidinedione derivative with the molecular formula C6H10N2O2S. It is a heterocyclic organic compound that contains a sulfur atom and a 2-sulfanylpropan-2-yl group. (5S)-5-(2-sulfanylpropan-2-yl)imidazolidine-2,4-dione has been studied for its potential pharmaceutical applications, particularly in the treatment of diabetes and related metabolic disorders.

77210-10-7

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77210-10-7 Usage

Uses

Used in Pharmaceutical Industry:
(5S)-5-(2-sulfanylpropan-2-yl)imidazolidine-2,4-dione is used as a potential therapeutic agent for the treatment of diabetes and related metabolic disorders. Its specific properties and potential uses would need to be further investigated through experimental studies and clinical trials to confirm its efficacy and safety in treating these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 77210-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,1 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77210-10:
(7*7)+(6*7)+(5*2)+(4*1)+(3*0)+(2*1)+(1*0)=107
107 % 10 = 7
So 77210-10-7 is a valid CAS Registry Number.

77210-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (5S)-5-(2-sulfanylpropan-2-yl)imidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names (S)-(+)-5-(1-mercapto-1-methyl)ethylhydantoin

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:77210-10-7 SDS

77210-10-7Downstream Products

77210-10-7Relevant academic research and scientific papers

Search for pro-drug forms of D-penicillamine: Synthesis and metabolism of D-pen-hydantoin.

Poupaert,Mukarugambwa,Dumont

, p. 511 - 514 (2007/10/02)

The existence of dihydropyrimidase possessing the ability to hydrolyse into hydantoic acids some hydantoins of D relative configuration has been pointed out in the literature. Owing to the identity of relative configuration between (R)-5-isopropylhydantoin and (S)-5(1-mercapto-1-methyl) ethylhydantoin (D-pen-hydantoin), the synthesis and metabolism study of the latter were undertaken to determine if D-penhydantoin could act as a pro-drug form of D-penicillamine. Various references compounds i.e. corresponding hydantoic acid, its disulfide and hydantoin disulfide were synthesized to perform a quantitative study of the metabolic profile of D-penhydantoin. The only metabolite detected in the urines of rat and rabbit was 5-isopropylidenehydantoin.

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