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1142-29-6

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1142-29-6 Usage

Uses

4-(3-allylthioureido)benzoic acid is used as a reactant in the preparation of new ecologically safe alkyl oxo(thione)tetrahydroquinazolines, alkylthioureidobenzoic acids and their alkyl esters, with cytokinin activity.

Check Digit Verification of cas no

The CAS Registry Mumber 1142-29-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1142-29:
(6*1)+(5*1)+(4*4)+(3*2)+(2*2)+(1*9)=46
46 % 10 = 6
So 1142-29-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O2S/c1-2-7-12-11(16)13-9-5-3-8(4-6-9)10(14)15/h2-6H,1,7H2,(H,14,15)(H2,12,13,16)

1142-29-6SDS

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 4-(prop-2-enylcarbamothioylamino)benzoic acid

1.2 Other means of identification

Product number -
Other names 1-allyl-3-(4-carboxyphenyl)-2-thiourea

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:1142-29-6 SDS

1142-29-6Downstream Products

1142-29-6Relevant articles and documents

Synthesis, characterization, and antibacterial activity of some thiazoles derived from allyl thioureas

Khare,Sharma,Sharma

, p. 702 - 707 (2016)

Synthesis of thiazoles was carried out from allyl thioureas using different cyclizing agents such as hydrogen chloride gas and bromine. Synthesized compounds were characterized by IR, 1H and 13C NMR, mass spectrometry, and elemental analysis. The synthesized thiazoles were evaluated for their antibacterial activity against Gram postitive (Lactobacillus bulgaris and Streptococcus mitis) and Gram negative (Yersinia) as well as antifungal activity against Aspergillus niger fungi.

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