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Benzoic acid, 2-[[[(4-methylphenyl)amino]carbonyl]amino]-, is a complex organic compound with the chemical formula C15H16N2O3. It is a derivative of benzoic acid, featuring a 4-methylphenyl group attached to the amino group, which is further connected to a carbonyl group and another amino group. Benzoic acid, 2-[[[(4-methylphenyl)amino]carbonyl]amino]- is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various drugs. Its structure allows for the formation of salts with different cations, which can influence its solubility and biological activity. The compound's specific properties and reactivity make it a valuable component in the development of new medications and therapeutic agents.

1566-76-3

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1566-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1566-76-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1566-76:
(6*1)+(5*5)+(4*6)+(3*6)+(2*7)+(1*6)=93
93 % 10 = 3
So 1566-76-3 is a valid CAS Registry Number.

1566-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-p-Tolyl-N'-o-carboxyphenyl-harnstoff

1.2 Other means of identification

Product number -
Other names N-(p-Tolylcarbamoyl)-anthranilsaeure

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:1566-76-3 SDS

1566-76-3Relevant academic research and scientific papers

Efficient preparation of 3-substituted quinazolinediones directly from anthranilic acids and isocyanates

Koay, Natalie,Campeau, Louis-Charles

experimental part, p. 473 - 478 (2011/05/14)

An efficient and practical synthesis of 3-substituted quinazolinediones is described. The protocol uses readily available isocyanates and anthranilic acids as precursors in a one-pot operation and has been demonstrated on >50 g scale. Isolation of the pro

Convenient Preparation of N-substituted 2-Amino-4H-3,1-benzoxazin-4-ones and 3-Substituted 2,4(1H,3H)-Quinazolinediones

Papadopoulos, E. P.,Torres, C. D.

, p. 269 - 272 (2007/10/02)

Room temperature of 2-(3-arylureido)benzoic acids (1) and methyl2-(3-alkyl-, or 3-arylureido)-benzoates (2) with concentrated sulfuric acid leads to N-substituted 2-amino-4H-3,1-benzoxazin-4-ones (3) in generally very good yields.The isomeric 3-substitute

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