3364-82-7 Usage
General Description
(4-Oxothiazolidin-2-ylidene)acetonitrile, also known as OTAN, is a chemical compound with the molecular formula C5H4N2OS. It is a highly reactive and versatile compound, commonly used in organic synthesis for the preparation of new pharmaceuticals, agrochemicals and materials. OTAN has been studied for its potential antimicrobial and antiviral activities. It is also used as a building block in the synthesis of various heterocyclic compounds. OTAN possesses a thiazolidin-2-ylidene moiety, which imparts unique reactivity and functional group compatibility, making it a valuable intermediate in the synthesis of diverse chemical compounds. Overall, (4-Oxothiazolidin-2-ylidene)acetonitrile is an important chemical building block with versatile applications in industrial and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 3364-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3364-82:
(6*3)+(5*3)+(4*6)+(3*4)+(2*8)+(1*2)=87
87 % 10 = 7
So 3364-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N2OS/c6-2-1-5-7-4(8)3-9-5/h1H,3H2,(H,7,8)/b5-1+
3364-82-7Relevant articles and documents
Synthesis and DNase I inhibitory properties of some 4-thiazolidinone derivatives
Kolarevi?, Ana,Ili?, Budimir S.,Koci?, Gordana,D?ambaski, Zdravko,?melcerovi?, Andrija,Bond?i?, Bojan P.
, p. 264 - 274 (2019)
Twelve new thiazolidinones were synthesized and, together with 41 previously synthesized thiazolidinones,?evaluated for inhibitory activity against deoxyribonuclease I (DNase I) in vitro. Ten compounds inhibited commercial bovine pancreatic DNase I with a
Reactions of transition metal carbonyl anions with 2-(1-bromoalkylidene) thiazolidin-4-ones: Halogenophilic attack or deprotonation
Sazonov,D?ambaski,Shtern,Markovi?,Beletskaya
experimental part, p. 29 - 33 (2011/02/25)
Bromophilic attack by the transition metal carbonyl anion, [Re(CO) 5]Na (pKa = 21.1), on 2-(1-bromoalkylidene)thiazolidin-4- ones is significantly faster than abstraction of an acidic lactam hydrogen (pKa ～17-18), when the
