27799-80-0 Usage
General Description
1-(o-Methoxybenzyl)-1H-benzotriazole is an organic chemical compound with the molecular formula C14H13N3O. It is often used as a stabilizer and UV absorber in a variety of materials, including plastics, polymers, coatings, and adhesives. 1-(o-Methoxybenzyl)-1H-benzotriazole is known for its ability to protect against the damaging effects of ultraviolet radiation, making it a valuable additive in products that are exposed to sunlight and other sources of UV light. Additionally, 1-(o-Methoxybenzyl)-1H-benzotriazole has been found to possess antioxidant properties, further enhancing its utility in preserving the integrity and longevity of various materials. Its diverse applications and beneficial properties make it a valuable chemical in the manufacturing and maintenance of a wide range of products.
Check Digit Verification of cas no
The CAS Registry Mumber 27799-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,7,9 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27799-80:
(7*2)+(6*7)+(5*7)+(4*9)+(3*9)+(2*8)+(1*0)=170
170 % 10 = 0
So 27799-80-0 is a valid CAS Registry Number.
27799-80-0Relevant articles and documents
Facile one-pot synthesis of N-alkylated benzimidazole and benzotriazole from carbonyl compounds
Meng, Xu,Li, Xiaolong,Chen, Wenlin,Zhang, Yuanqing,Wang, Wen,Chen, Jinying,Song, Jinli,Feng, Huijie,Chen, Baohua
, p. 349 - 356 (2014/04/17)
An efficient one-pot N-alkylation of benzimidazole and benzotriazole from carbonyl compounds and tosylhydrazide has been accomplished via copper powder-catalyzed N - H bond insertion affording N-alkylated products in good yields. The reaction can tolerate a wide range of carbonyl compounds, such as aryl, alkyl, heterocyclic and α,β-unsaturated ketones, and aldehydes.
Mitsunobu reaction of 1,2,3-NH-triazoles: A regio- and stereoselective approach to functionalized triazole derivatives
Yan, Wuming,Liao, Tao,Tuguldur, Odbadrakh,Zhong, Cheng,Petersen, Jeffrey L.,Shi, Xiaodong
supporting information; experimental part, p. 2720 - 2724 (2012/06/01)
The Mitsunobu reaction was used in the preparation of chiral triazole derivatives. The reactions gave good to excellent yields with large substrate scope. Complete stereochemistry inversion was obtained, making this strategy one practical approach for the
