1225041-15-5 Usage
General Description
6-nitro-2-(Trifluoromethyl)benzothiazole is a chemical compound with the molecular formula C8H4F3NOS2. It is a nitro-substituted benzothiazole derivative with a trifluoromethyl group attached to the second position of the benzothiazole ring. 6-nitro-2-(Trifluoromethyl)benzothiazole is used in the synthesis of pharmaceuticals and agrochemicals, as well as in research and development of new materials. It has potential applications in the fields of medicinal chemistry, materials science, and organic synthesis. 6-nitro-2-(Trifluoromethyl)benzothiazole has been studied for its antimicrobial and antifungal properties, and it also possesses potential as a fluorescent probe for metal ion sensing. Overall, this chemical compound has a wide range of potential applications and is of interest to researchers in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1225041-15-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,0,4 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1225041-15:
(9*1)+(8*2)+(7*2)+(6*5)+(5*0)+(4*4)+(3*1)+(2*1)+(1*5)=95
95 % 10 = 5
So 1225041-15-5 is a valid CAS Registry Number.
1225041-15-5Relevant articles and documents
Switching reaction pathways of trifluoromethylated thiobenzanilides by choice of different oxidative systems
Zhu, Jiangtao,Xie, Haibo,Li, Shan,Chen, Zixian,Wu, Yongming
, p. 306 - 309 (2011/06/20)
Trifluoromethylated thiobenzanilides are efficiently converted to 2-trifluoromethylbenzothiazoles via intramolecular oxidative cyclization under CAN/NaHCO3 oxidation, while the dimerized products with "-S-S-" bond linkage are obtained when PIDA
A general and straightforward method for the synthesis of 2-trifluoromethylbenzothiazoles
Zhu, Jiangtao,Chen, Zixian,Xie, Haibo,Li, Shan,Wu, Yongming
supporting information; experimental part, p. 2434 - 2436 (2010/07/10)
An efficient one-pot method for the synthesis of 2- trifluoromethylbenzothiazoles by the treatment of trifluoromethylimidoyl chlorides with sodium hydrosulfide hydrate using PdCl2 as the sole catalyst in DMSO is described. The reaction proceeds via thiolation/C-H bond functionalization/C-S bond formation in moderate to high yields with good functional group tolerance.
