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7245-61-6

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7245-61-6 Usage

General Description

(3-Benzoyl-thioureido)-acetic acid is a chemical compound that contains both a benzoyl group and a thiourea moiety. It is a white powder with a molecular formula of C11H10N2O3S and a molecular weight of 250.27 g/mol. (3-BENZOYL-THIOUREIDO)-ACETIC ACID has been studied for its potential biological activities, including antimicrobial and antitumor properties. It is used in pharmacological and medicinal research as a potential drug candidate. Additionally, (3-Benzoyl-thioureido)-acetic acid may have applications in the field of organic synthesis and materials science due to its unique chemical structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 7245-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,4 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7245-61:
(6*7)+(5*2)+(4*4)+(3*5)+(2*6)+(1*1)=96
96 % 10 = 6
So 7245-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O3S/c13-8(14)6-11-10(16)12-9(15)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14)(H2,11,12,15,16)/p-1

7245-61-6Relevant articles and documents

Characterization and Computational Studies of 2-(Benzamido)Thiazol-5-yl Benzoate

Odame,Hosten,Betz,Lobb,Tshentu

, p. 136 - 142 (2019/05/04)

2-(Benzamido)thiazolylbenzoate is synthesized via a novel method. It is characterized by spectroscopy, micranalysis, and GC-MS. It crystallizes in the monoclinic space group P21/n with a = 19.8990(5), b = 7.3680(2), c = 22.3845(6) ?, β = 113.799(1)°, V = 3002.85(14) ?3Z = 8. The HOMO-LUMO of the reactants and products are considered.

Synthesis and characterization of N-benzoyl-N′-carboxyalkyl substituted thiourea derivatives

Li, Zhonghua,Zhang, Yan,Wang, Yangang

, p. 293 - 297 (2007/10/03)

N-Benzoyl-N′-carboxyl substituted thiourea derivatives (I-X) have been synthesized by the reaction of benzoyl isothiocyanate with amino acids. Their structures are confirmed by IR, 1HNMR, and elemental analysis. The reaction conditions are expe

Synthesis and biological activity of N-aroyl-N'-carboxyalkyl thiourea derivatives

Zhang, You-Ming,Wei, Tai-Bao,Wang, Xiu-Chun,Yang, Su-You

, p. 604 - 606 (2007/10/03)

Ten new N-aroyl-N'-carboxyalkyl thiourea derivatives have been prepared in modest to good yield via the reaction of aroyl isothiocyanates and amino acids.The products have been characterized on the basis of analytical and spectral (IR and 1H NMR) data.The promoting effects of some of the compounds on wheat growth have been tested preliminary.

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