975-21-3 Usage
Description
(2E)-2-[(4,9-dimethoxy-5-oxo-5H-furo[3,2-g]chromen-7-yl)methylidene]hydrazinecarbothioamide, also known as furocoumarin-hydrazinecarbothioamide, is a potent bioactive compound derived from furocoumarin, a class of natural compounds found in certain plants. It is known for its diverse pharmacological properties, including anti-inflammatory, antimicrobial, and anticancer activities. (2E)-2-[(4,9-dimethoxy-5-oxo-5H-furo[3,2-g]chromen-7-yl)methylidene]hydrazinecarbothioamide's structure consists of a furan ring fused to a coumarin ring, and it has a hydrazinecarbothioamide functional group, which contributes to its reactivity and biological activity.
Used in Pharmaceutical Industry:
(2E)-2-[(4,9-dimethoxy-5-oxo-5H-furo[3,2-g]chromen-7-yl)methylidene]hydrazinecarbothioamide is used as a potential therapeutic agent for its diverse pharmacological properties, including anti-inflammatory, antimicrobial, and anticancer activities. Its unique structure and hydrazinecarbothioamide functional group contribute to its reactivity and biological activity, making it a promising candidate for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 975-21-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,7 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 975-21:
(5*9)+(4*7)+(3*5)+(2*2)+(1*1)=93
93 % 10 = 3
So 975-21-3 is a valid CAS Registry Number.
975-21-3Relevant articles and documents
Synthesis and anticonvulsant activity of new thiazolidinone and thioxoimidazolidinone derivatives derived from furochromones
Ragab,Eid,El-Tawab
, p. 926 - 929 (2007/10/03)
Various new thiazolidinone and thioxoimidazolidinone derivatives were synthesized starting from 4,9-dimethoxy-5H-furo[3,2-g][1]benzopyran-5-on-7-carboxaldehyde. The anticonvulsant activity of the synthesized compounds was evaluated. Most of the compounds showed anticonvulsant activity equal or superior to phenobarbital.
