376585-97-6 Usage
General Description
4-Bromo-2-isopropyl-1,3-thiazole is a chemical compound with the molecular formula C6H9BrN2S. This makes it a member of the group of organic substances known as thiazoles, which are aromatic heterocyclic compounds with a five-membered ring containing four carbon atoms and one sulfur atom, and also an atom of nitrogen at the position 1. The 4-Bromo-2-isopropyl-1,3-thiazole is characterized by the presence of a bromine atom and an isopropyl group attached to different carbon atoms of the thiazole ring. As is the case with many organic substances, the synthetic routes, properties, reactivity, and possible applications of this substance are determined by the structure of the molecule, which gives it a particular set of chemical and physical properties. It is used in various lab-based scientific research experiments.
Check Digit Verification of cas no
The CAS Registry Mumber 376585-97-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,6,5,8 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 376585-97:
(8*3)+(7*7)+(6*6)+(5*5)+(4*8)+(3*5)+(2*9)+(1*7)=206
206 % 10 = 6
So 376585-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H8BrNS/c1-4(2)6-8-5(7)3-9-6/h3-4H,1-2H3
376585-97-6Relevant articles and documents
Total synthesis of cystothiazole A by microwave-assisted olefin cross-metathesis
Gebauer, Julian,Arseniyadis, Stellios,Cossy, Janine
, p. 2701 - 2704 (2008)
A short and convergent synthesis of the myxobacterial antibiotic cystothiazole A by a microwave-assisted olefin crossmetathesis reaction and a sequential microwave-assisted cross-metathesis/Stille coupling is described. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
Synthesis of 2′-substituted 4-bromo-2,4′-bithiazoles by regioselective cross-coupling reactions
Bach, Thorsten,Heuser, Stefan
, p. 5789 - 5795 (2007/10/03)
The synthesis of the title compounds (1) was achieved in two steps starting from readily available 2,4-dibromothiazole (2). In a regioselective Pd(O)-catalyzed cross-coupling step, compound 2 was converted into a variety of 2-substituted 4-bromothiazoles
