66277-05-2 Usage
Description
2-BENZOTHIAZOL-2-YL-2-METHYLPROPIONITRILE is a chemical compound characterized by the molecular formula C11H9NOS. It is recognized for its role as a photoinitiator in the polymer and resin industry, facilitating the photopolymerization process. 2-BENZOTHIAZOL-2-YL-2-METHYLPROPIONITRILE is also utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, highlighting its versatility in chemical applications.
Uses
Used in Polymer and Resin Industry:
2-BENZOTHIAZOL-2-YL-2-METHYLPROPIONITRILE is used as a photoinitiator for its ability to initiate and accelerate the photopolymerization process. This makes it a valuable component in the production of coatings and adhesives, contributing to the development of various industrial applications.
Used in Pharmaceutical and Agrochemical Synthesis:
As an intermediate, 2-BENZOTHIAZOL-2-YL-2-METHYLPROPIONITRILE plays a crucial role in the synthesis of pharmaceuticals and agrochemicals. Its involvement in these processes underscores its importance in creating a range of products that serve different sectors.
It is important to handle 2-BENZOTHIAZOL-2-YL-2-METHYLPROPIONITRILE with care due to its potential hazards. Ingestion or inhalation may be harmful, and it can cause skin and eye irritation, necessitating proper safety measures during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 66277-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,7 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66277-05:
(7*6)+(6*6)+(5*2)+(4*7)+(3*7)+(2*0)+(1*5)=142
142 % 10 = 2
So 66277-05-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2S/c1-11(2,7-12)10-13-8-5-3-4-6-9(8)14-10/h3-6H,1-2H3
66277-05-2Relevant articles and documents
Di- tert-butyl Peroxide-Mediated Radical C(sp2/sp3)-S Bond Cleavage and Group-Transfer Cyclization
Luo, Kai,Yang, Wen-Chao,Wei, Kai,Liu, Yue,Wang, Jun-Ke,Wu, Lei
, p. 7851 - 7856 (2019/10/11)
A novel strategy of cascade radical C(sp2/sp3)-S bond cleavage and group-transfer cyclization is disclosed. Triggered by alkyl radicals, varieties of 2-isocyanoaryl thioethers containing aliphatic, aryl, and heteroaromatic groups can be cleaved and precisely reinstalled to give benzothiazole derivatives. Mechanistic studies reveal that the cascade reaction undertakes an intermolecular pathway, and the inner radical sources (R radicals) exhibit high priority over those of methyl radical origin from di-tert-butyl peroxide.
