7245-61-6

Usage

Uses

Used in Pharmaceutical and Medicinal Research:
(3-Benzoyl-thioureido)-acetic acid is used as a potential drug candidate due to its demonstrated biological activities, including antimicrobial and antitumor properties. Its unique chemical structure and reactivity contribute to its potential as a therapeutic agent in various medical applications.
Used in Organic Synthesis:
(3-Benzoyl-thioureido)-acetic acid may have applications in the field of organic synthesis, where its unique chemical structure can be utilized to create new compounds with specific properties.
Used in Materials Science:
Additionally, (3-Benzoyl-thioureido)-acetic acid may find use in materials science, where its reactivity and chemical structure could be employed to develop new materials with tailored characteristics for various industries.

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

Upstream product

• 21406-30-4 N-Benzoylamino-dithiokohlensaeuremethylester 
• 56-40-6 glycine 
• 58328-36-2 N,N-diethyl-N'-benzoyl-thiourea 
• 333-20-0 potassium thioacyanate 
• 98-88-4 benzoyl chloride 
• 6287-87-2 benzoyldithiocarbamic acid ethyl ester 
• 64-17-5 ethanol 
• 532-55-8 Benzoyl isothiocyanate 

Downstream Products

• 503-87-7 2-thiohydantoin 
• 1350889-13-2 2-(tert-butylamino)-1-(4-chlorophenyl)-2-oxoethyl-2-(3-benzoylthioureido)acetate 
• 1350889-24-5 1-(cyclohexylamino)-2-methyl-1-oxopropan-2-yl-2-(3-benzoylthioureido)acetate 
• 211098-35-0 Cu₂(C₁₀H₉N₂O₃S)2Cl₂ 
• 211098-37-2 Zn₂(C₁₀H₉N₂O₃S)2(OH)2 

Relevant academic research and scientific papers

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

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.

Ugi reaction of thiouridocarboxylic acids: A synthesis of thiourea-peptoids

Benzoylthioureidocarboxylic acids, prepared from benzoyl chlorides, potassium thiocyanate, and α-aminoacids, are used as acid components in the Ugi reaction to produce thiourea-peptoids in moderate to good yields.

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

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 of 1-benzoyl-3-alkylthioureas by transamidation under microwave in dry media

1-Benzoyl-3,3-diethylthiourea was transamidated with several amines to the corresponding 1-benzoyl-3-alkylthioureas in open vessels under microwave irradiation using a domestic oven. The syntheses were performed in solvent- free conditions on potassium fluoride impregnated alumina. Yields were dramatically improved in comparison with classical heating under the same conditions. (C) 2000 Published by Elsevier Science Ltd.

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

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.