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S-phenyl butylthiocarbamate, also known as phenylbutyl isothiocyanate or phenylbutyl thiocarbamate, is an organic compound with the chemical formula C11H13NS. It is a colorless to pale yellow liquid with a pungent odor and is soluble in organic solvents. This chemical is primarily used as a synthetic intermediate in the production of pharmaceuticals, agrochemicals, and other chemical products. It is also known for its potential role as a chemopreventive agent in cancer research due to its ability to induce phase II detoxification enzymes. However, it is important to note that S-phenyl butylthiocarbamate can be harmful if ingested or inhaled, and it may cause skin and eye irritation.

4910-31-0

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4910-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4910-31-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4910-31:
(6*4)+(5*9)+(4*1)+(3*0)+(2*3)+(1*1)=80
80 % 10 = 0
So 4910-31-0 is a valid CAS Registry Number.

4910-31-0SDS

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 S-phenyl N-butylcarbamothioate

1.2 Other means of identification

Product number -
Other names Carbamothioic acid,butyl-,S-phenyl ester

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:4910-31-0 SDS

4910-31-0Downstream Products

4910-31-0Relevant academic research and scientific papers

Synthesis of thiocarbamates from thiols and isocyanates under catalyst- and solvent-free conditions

Movassagh, Barahman,Soleiman-Beigi, Mohammad

, p. 137 - 140 (2008/09/20)

A simple and efficient procedure was developed for the synthesis of S-alkyl (aryl) thiocarbamates under solvent-free conditions without the use of a catalyst. The significant features of this protocol are (a) operational simplicity, (b) mild reaction cond

N-Nitroso Compounds. IV. Reaction of N-Nitrosourea with Thiol. A New Synthesis of Thiocarbamic S-Esters

Yoshida, Kitaro,Isobe, Masayoshi,Yano, Kazuyuki,Nagamatsu, Kazuo

, p. 2143 - 2144 (2007/10/02)

Thirteen thiocarbamic S-esters have been prepared in good yield by the reaction of thiol with substituted N-methyl-N-nitrosourea in anhydrous acetonitrile.

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