1435-01-4

Basic information

• Product Name: Hydrazinecarbothioamide, N-phenyl-2-(2-thienylmethylene)-
• CAS NO: 1435-01-4
• Molecular Formula: C12H11N3S2
• Molecular Weight: 261.371
• Mol File: 1435-01-4.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Hydrazinecarbothioamide, N-phenyl-2-(2-thienylmethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarbothioamide, N-phenyl-2-(2-thienylmethylene)-(1435-01-4)
• EPA Substance Registry System: Hydrazinecarbothioamide, N-phenyl-2-(2-thienylmethylene)-(1435-01-4)

Safety Data

• Hazardous Substances Data: 1435-01-4(Hazardous Substances Data)

Usage

General Description

Hydrazinecarbothioamide, N-phenyl-2-(2-thienylmethylene)- is a chemical compound with a unique structure, consisting of a hydrazinecarbothioamide group with a phenyl and 2-thienylmethylene substitution. It is used as a building block in organic synthesis, primarily in the pharmaceutical and agricultural industries. Hydrazinecarbothioamide, N-phenyl-2-(2-thienylmethylene)- has been studied for its potential biological and pharmacological activities, including its antifungal and antimicrobial properties. Its unique structure and potential applications make it an interesting target for further research and development in the fields of medicine and agriculture.

Upstream product

• 98-03-3 thiophene-2-carbaldehyde 
• 5351-69-9 4-Phenyl-3-thiosemicarbazide 
• 62-53-3 aniline 
• 103-72-0 phenyl isothiocyanate 
• 26152-25-0 methyl 1-(thiophene-2-ylmethylene)-hydrazinecarbodithioate 

Downstream Products

• 1026792-44-8 N-phenyl-5-(thiophen-2-yl)-1,3,4-thiadiazole-2-amine 
• 1093399-56-4 4-amino-2,7-dinitro-4'-phenylspiro(fluoren-9,3'-[1,2,4]triazolidine)-5'-thione-1-(thiophen-2-carbonyl) 
• 84409-01-8 4-amino-2,7-dinitro-9-fluorenone 
• 1093399-50-8 [4-phenyl-1-(thiophen-2-carbonyl)-3-thioxo-1,2,4-triazaspiro[4.5]deca-6,9-dien-8-ylidene]malononitrile 
• 1093399-44-0 4a-hydroxy-3-(thiophene-2-yl)indeno[1,2-e][1,3,4]oxadiazine-9(4aH)-one 
• 1093399-45-1 3-cyano-4-oxo-N-phenylideno[1,2-c]pyrazole-1(4H)-carbothioamide 
• 1174196-53-2 Ni(C₄H₃S(CHNNC(S)NHC₆H₅))2 
• 110591-16-7 Cu(C₄H₃S(CHNNC(S)NHC₆H₅))2 
• 110591-15-6 [Zn(Httsc-N-Ph)₂] 
• 47107-74-4 tetrameric (triphenylphosphine)copper(I) iodide 

Relevant articles and documents

Inhibitory effect of synthetic aromatic heterocycle thiosemicarbazone derivatives on mushroom tyrosinase: Insights from fluorescence, 1H NMR titration and molecular docking studies

Three structurally similar aromatic heterocyclic compounds 2-thiophenecarboxaldehyde (a), 2-furaldehyde (b), 2-pyrrolecarboxaldehyde (c) were chosen and a series of their thiosemicarbazone derivatives(1a-3a, 1b-3b and 1c-3c) were synthesized to evaluate t

Efficient synthesis of novel 2,3-dihydro-1,3,5,4-thiadiazaphosphole derivatives

ABSTRACT: The condensation of various thiosemicarbazones with methyl thiophene-2-carboximidate afforded the corresponding intermediates 2a–2h. Subsequent cyclization of the latter compounds with hexamethylphosphorous triamide constitutes a new route to the synthesis of novel highly functionalized thiadiazaphosphole derivatives 4a–4h. This method offers significant advantages such as efficiency, high yields and mild reaction conditions.

Ion flotation and flame atomic absorption spectrophotometric determination of nickel and cobalt in environmental and pharmaceutical samples using a thiosemicarbazone derivative

THIOPHENE-2-Carboxaldhyde-4-Phenyl thiosemicarbazone (TAPT), a NS containing ligand, combines with Ni (II) and Co (II) each individually and in combination, to form complexes in aqueous solution. These complexes could be successfully separated by a surfac