690632-35-0 Usage
Uses
Used in Pharmaceutical Industry:
[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methanamine hydrochloride is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique chemical structure allows for the creation of new drugs with potential therapeutic applications, such as antibiotics, anti-inflammatory agents, and other medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, [2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methanamine hydrochloride is utilized as a precursor in the synthesis of agrochemicals, including pesticides and herbicides. Its properties contribute to the development of effective and targeted solutions for crop protection and management.
Used in Organic Chemistry Research:
[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methanamine hydrochloride is also used as a research compound in organic chemistry. Its unique structure and properties make it a valuable tool for studying chemical reactions, mechanisms, and the development of new synthetic methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 690632-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,0,6,3 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 690632-35:
(8*6)+(7*9)+(6*0)+(5*6)+(4*3)+(3*2)+(2*3)+(1*5)=170
170 % 10 = 0
So 690632-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClN2S.ClH/c11-8-3-1-7(2-4-8)10-13-9(5-12)6-14-10;/h1-4,6H,5,12H2;1H
690632-35-0Relevant academic research and scientific papers
Huang, Danling,Zheng, Shumin,Zhang, Tianyuan,Cheng, Yong-Xian
, (2021)
A series of (-)-borneol derivatives containing 2-aryl-thiazole scaffold were designed, synthesized, and characterized by 1H NMR, 13C NMR, and HRMS. The fungicidal activities of these novel compounds against Fusarium oxysporum, Magnaporthe grisea, Botrytis cinerea, and Penicillium digitatum were evaluated. The results indicated that (1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl(Z)-4-oxo-4-(((2-phenylthiazol-4-yl)methyl)amino)but-2-enoate (6a) displayed potential fungicidal activities with broad spectrum. Especially, 6a exhibited an IC50 value of 48.5 mg/L against P. digitatum, which has higher fungicidal activity than commercial products hymexazol and amicarthiazol. Moreover, (1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl-4-oxo-4-(((2-phenylthiazol-4-yl)methyl)amino)butanoate (5a) possesses an IC50 value of 24.3 mg/L against B. cinerea, comparable to hymexazol and far superior to amicarthiazol. Furthermore, the superficial structure–activity relationship was discussed, which might be helpful for discovering novel fungicides.
