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Sec-Butyl-thiourea, also known as 2-(1-methylpropyl)-1,3-thiazolidine-2,4-dione, is an organic compound with the chemical formula C6H12N2OS. It is a colorless to pale yellow crystalline solid that is soluble in water and various organic solvents. SEC-BUTYL-THIOUREA is primarily used as a rubber accelerator, promoting the vulcanization process in rubber manufacturing, and as a corrosion inhibitor in various industrial applications. It is also known for its potential applications in the pharmaceutical and agricultural sectors. However, due to its potential health and environmental risks, its use is regulated in many countries.

6814-99-9

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6814-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6814-99-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,1 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6814-99:
(6*6)+(5*8)+(4*1)+(3*4)+(2*9)+(1*9)=119
119 % 10 = 9
So 6814-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2S/c1-3-4(2)7-5(6)8/h4H,3H2,1-2H3,(H3,6,7,8)

6814-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name butan-2-ylthiourea

1.2 Other means of identification

Product number -
Other names N-2-butylthiourea

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:6814-99-9 SDS

6814-99-9Relevant academic research and scientific papers

Process for preparing 2-aminothiazole-5-carboxamides useful as kinase inhibitors

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Page/Page column 13, (2008/06/13)

The invention is directed to processes for preparing 2-aminothiazole-5-carboxamides of formula I [image] wherein R1, R2, R3, R4 and R5 are as defined as set forth in the specification herein.

A convenient and efficient method for the synthesis of mono- and N,N-disubstituted thioureas

Kodomari, Mitsuo,Suzuki, Masato,Tanigawa, Keiko,Aoyama, Tadashi

, p. 5841 - 5843 (2007/10/03)

A convenient method for the synthesis of mono- and N,N-disubstituted thioureas by the debenzoylation of N-substituted- and N,N-disubstituted- N′-benzoylthioureas with hydrazine hydrate under solvent-free conditions has been developed. N-Substituted-N′-benzoylthioureas and hydrazine hydrate were mixed, and stirred at room temperature without a solvent to give the corresponding N-substituted thioureas in high yields.

PROCESS FOR PREPARING 2-AMINOTHIAZOLE-5-AROMATIC CARBOXAMIDES AS KINASE INHIBITORS

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Page/Page column 46-47, (2008/06/13)

The invention relates to processes for preparing compounds having the formula (I) and crystalline forms thereof, wherein Ar is aryl or heteroaryl, L is an optional alkylene linker, and R2, R3, R4, and R5, are as defined in the specification herein, which compounds are useful as kinase inhibitors, in particular, inhibitors of protein tyrosine kinase and p38 kinase.

THIAZOLE DERIVATIVES AND USE THEREOF

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Page/Page column 165, (2008/06/13)

The present invention is related to thiazole derivatives of Formula (I) in particular for the treatment and/or prophylaxis of autoimmune disorders and/or inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, bacterial or viral infections, kidney diseases, platelet aggregation, cancer, transplantation, graft rejection or lung injuries.

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