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N-(3-phenylprop-2-en-1-yl)benzenecarbothioamide is a chemical compound with the molecular formula C16H13NS. It is an organic compound that belongs to the class of thioamides, which are derivatives of amides where the oxygen atom is replaced by a sulfur atom. This particular compound features a benzene ring (C6H5) attached to a thioamide group (-CNH-S) and a 3-phenylprop-2-en-1-yl group, which is a phenylpropene side chain with a double bond. The compound is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as its use as an intermediate in the preparation of various organic compounds. Its chemical structure and properties make it a versatile building block in organic synthesis, particularly in the development of new molecules with specific biological activities.

7472-35-7

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7472-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7472-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7472-35:
(6*7)+(5*4)+(4*7)+(3*2)+(2*3)+(1*5)=107
107 % 10 = 7
So 7472-35-7 is a valid CAS Registry Number.

7472-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(Z)-3-phenylprop-2-enyl]benzenecarbothioamide

1.2 Other means of identification

Product number -
Other names N-Cinnamyl-benzthionamid

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 -
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More Details:7472-35-7 SDS

7472-35-7Downstream Products

7472-35-7Relevant academic research and scientific papers

Lewis Base/Br?nsted Acid Cocatalysis for Thiocyanation of Amides and Thioamides

Qumruddeen,Yadav, Arun,Kant, Ruchir,Tripathi, Chandra Bhushan

, p. 2814 - 2822 (2020/01/31)

Lewis base/Br?nsted acid cocatalysis for electrophilic thiocyanation of olefins is reported. Using a combination of triphenylphosphine selenide and diphenyl phosphate as a catalyst, a wide range of unsaturated amides and thioamides underwent thiocyanation to furnish thiocyanated thiazoline and oxazoline derivatives in high yields (up to 97%).

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