834861-72-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(3-CHLOROPHENYL)THIOACETAMIDE is used as a pharmaceutical candidate for its potential antimicrobial and antifungal properties. It can be utilized in the development of new drugs to combat various infections caused by bacteria and fungi.
Used in Organic Synthesis:
2-(3-CHLOROPHENYL)THIOACETAMIDE is used as a building block in the synthesis of other organic compounds. Its unique structure allows it to be a valuable component in the creation of new molecules with various applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 834861-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,4,8,6 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 834861-72:
(8*8)+(7*3)+(6*4)+(5*8)+(4*6)+(3*1)+(2*7)+(1*2)=192
192 % 10 = 2
So 834861-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNS/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4H,5H2,(H2,10,11)
834861-72-2Relevant articles and documents
THIAZOLE DERIVATIVE
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Page/Page column 131, (2012/12/14)
Provided is a compound having an agonist action on GPR52, which is useful as a prophylactic or therapeutic drug for mental diseases such as schizophrenia and the like, and the like. A compound represented by the formula (I): wherein each symbol is as defi
Histamine H1 receptor ligands. Part I. Novel thiazol-4-ylethanamine derivatives: Synthesis and in vitro pharmacology
Walczynski,Timmerman,Zuiderveld,Zhang,Glinka
, p. 533 - 541 (2007/10/03)
A series of 2-substituted thiazol-4-ylethanamines have been synthesized and tested for their histaminergic H1-receptor activities. The compounds with 2-phenyl substitution, regardless of the different physicochemical properties of the meta-substituents at the phenyl ring, showed weak H1-agonistic activity with pD2 values ranging from 4.35 to 5.36. When the phenyl group was replaced by a benzyl group, the resulting compounds all exhibited weak H1-antagonistic activity (pA2: 4.14-4.82). Copyright (C) 1999 Elsevier Science S.A.
