5351-83-7 Usage
Nitrothiophene group
Aromatic ring with a nitro group (-NO2) attached to a thiophene ring (a five-membered ring with a sulfur atom).
Hydrazinecarbothioamide moiety
A hydrazine (H2N-NH2) group connected to a carbothioamide group (a thioamide, which is a sulfur analog of an amide).
Potential applications
Organic synthesis and pharmaceuticals 2-[(5-nitrothiophen-2-yl)methylidene]hydrazinecarbothioamide may be used in the synthesis of other organic compounds and has potential applications in the development of new drugs.
Biological activities
The compound may exhibit various biological activities, such as抗菌, antiviral, or anticancer properties, which could make it useful in the treatment of various diseases and conditions.
Building block in drug development
The compound could be used as a starting material or intermediate in the development of new drugs, due to its unique structure and potential biological activities.
Ligand in coordination chemistry
2-[(5-nitrothiophen-2-yl)methylidene]hydrazinecarbothioamide may have properties that make it useful as a ligand, which are molecules that can bind to metal ions to form coordination complexes.
Reagent in organic reactions
The compound could be used as a reagent in organic reactions, such as catalysis or synthesis, due to its unique structure and potential reactivity.
Further research and testing
More studies and experiments are needed to fully understand the properties, potential applications, and limitations of 2-[(5-nitrothiophen-2-yl)methylidene]hydrazinecarbothioamide.
Check Digit Verification of cas no
The CAS Registry Mumber 5351-83-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5351-83:
(6*5)+(5*3)+(4*5)+(3*1)+(2*8)+(1*3)=87
87 % 10 = 7
So 5351-83-7 is a valid CAS Registry Number.
5351-83-7Relevant articles and documents
Novel inhibitors of tyrosinase produced by the 4-substitution of TCT
Xu, Jian,Liu, Jing,Zhu, Xinqi,Yu, Yanying,Cao, Shuwen
, p. 1530 - 1538 (2017)
We synthesized a series of 4- or 5-functionalized TCT derivatives (1?12) and investigated their inhibitory activities and mechanisms on tyrosinase by using Spectrofluorimetry, 1H and 13C NMR titration and IR spectra. The results of the fluorescence spectr
Synthesis and antiinflammatory activity of novel 2,5-disubstituted thiophene derivatives
Ibrahim Badr, Sahar Mohamed
experimental part, p. 131 - 143 (2011/12/05)
New series of 2,5-disubstituted thiophenes were synthesized. Thiosemicarbazones 1a-b were reacted with various reagents, such as diethyl-2-bromomalonate, ethyl-2-chloroacetoacetate, thioglycolic acid, 4-substituted phenacyl bromides, and acetic anhydride,
Synthesis and in vitro anti-leishmanial activity of 1-[5-(5-nitrofuran-2-yl)-1,3,4-thiadiazol-2-yl]- and 1-[5-(5-nitrothiophen-2-yl)-1,3,4-thiadiazol-2-yl]-4-aroylpiperazines
Behrouzi-Fardmoghadam, Mina,Poorrajab, Fatemeh,Ardestani, Sussan Kaboudanian,Emami, Saeed,Shafiee, Abbas,Foroumadi, Alireza
, p. 4509 - 4515 (2008/09/21)
The synthesis and anti-leishmanial activity of nitroheteroaryl-1,3,4-thiadiazole-based compounds including 1-[5-(5-nitrofuran-2-yl)-1,3,4-thiadiazol-2-yl]-4-aroylpiperazines and 1-[5-(5-nitrothiophen-2-yl)-1,3,4-thiadiazol-2-yl]-4-aroylpiperazines were described. Most of the synthesized compounds exhibited potent anti-leishmanial activity against both promastigote and amastigote forms of Leishmania major at non-cytotoxic concentrations. In general, 5-nitrofuran derivatives were more active than the corresponding 5-nitrothiophene analogues.
