4277-77-4 Usage
Uses
Used in Analytical Chemistry:
(2E)-2-benzylidene-N,1-dimethylhydrazinecarbothioamide is used as a reagent for the determination of metal ions, providing a means to detect and quantify their presence in various samples.
Used in Pharmaceutical Research:
(2E)-2-benzylidene-N,1-dimethylhydrazinecarbothioamide is being studied for its potential anti-cancer properties, as it has been found to inhibit the growth of certain cancer cells. This research aims to explore its therapeutic potential in oncology.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, (2E)-2-benzylidene-N,1-dimethylhydrazinecarbothioamide is being investigated for use in applications that require the control or prevention of microbial growth, such as in medical or industrial settings.
Used in Dye Production:
(2E)-2-benzylidene-N,1-dimethylhydrazinecarbothioamide is also used in the production of dyes, contributing to the coloration and quality of various products.
Used as a Chemical Intermediate:
In organic synthesis, (2E)-2-benzylidene-N,1-dimethylhydrazinecarbothioamide serves as a chemical intermediate, facilitating the synthesis of other compounds and contributing to the development of new chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 4277-77-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4277-77:
(6*4)+(5*2)+(4*7)+(3*7)+(2*7)+(1*7)=104
104 % 10 = 4
So 4277-77-4 is a valid CAS Registry Number.
4277-77-4Relevant academic research and scientific papers
Ring-chain tautomerism of N-substituted thiosemicarbazones
Zelenin,Kuznetsova,Alekseyev,Terentyev,Torocheshnikov,Ovcharenko
, p. 1257 - 1270 (2007/10/02)
The condensation products from 4,4-dimethyl- and 2,4,4-trimethylthiosemicarbazides and aldehydes or ketones, as well as those from 2-methyl- and 2,4-disubstituted thiosemicarbazides and aldehydes have the thiosemicarbazone structure, while ketones react with 2-methyl- or 2,4-dialkylthiosemicarbazides to form 1,2,4- triazolidine- 3-thiones. Both thiosemicarbazones and 1,2,4- triazolidine- 3-thiones in trifluoroacetic acid solution yield 1,3,4-thiadiazolidine-2-iminium salts. Their deprotonation by pyridine leads to thiosemicarbazones, including otherwise inaccessible 2-methyl- and 2,4-disubstituted ketone thiosemicarbazones. The mass-spectrometric investigation of these compounds also suggests presence of their tautomers in the gas phase.
