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4-Imidazolidinone, 3-amino-2-thioxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

117829-36-4

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117829-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117829-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,2 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 117829-36:
(8*1)+(7*1)+(6*7)+(5*8)+(4*2)+(3*9)+(2*3)+(1*6)=144
144 % 10 = 4
So 117829-36-4 is a valid CAS Registry Number.

117829-36-4SDS

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-amino-2-sulfanylideneimidazolidin-4-one

1.2 Other means of identification

Product number -
Other names 4-Imidazolidinone,3-amino-2-thioxo

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:117829-36-4 SDS

117829-36-4Relevant academic research and scientific papers

Cyclododecanone as a recyclable protecting group for the synthesis of highly functionalized 3-amino-2-thiohydantoins from conventional starting materials

Sathishkumar, Munusamy,Ramachandran, Gunasekar,Sathiyanarayanan, Kulathu Iyer

, p. 8498 - 8501 (2014)

A simple and efficient approach has been developed for the synthesis of highly substituted 3-amino-2-thiohydantoins using cyclododecanone as a protecting group and thiosemicarbazide, chloroacetic acid and substituted benzaldehyde as reactants. This high yielding (79-96%) protocol is a milder alternative to the traditional method that uses unprotected thiosemicarbazide. It was identified that the preferred pathway is the deprotection of 3-amino-2-thiohydantoins followed by the attack of chloroacetic acid on a secondary nitrogen with subsequent formation of the Knoevenagel product and its reaction with imine leading to the final product. The Royal Society of Chemistry.

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