499785-52-3 Usage
General Description
ETHYL 1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLATE is a chemical compound used in various industrial applications, including as a corrosion inhibitor in industrial water treatment and as a stabilizer in the production of polymers and coatings. It is a member of the benzotriazole family of compounds, which are known for their ability to inhibit corrosion and protect metal surfaces from degradation. This particular compound is characterized by its ethyl and carboxylate functional groups, which contribute to its ability to form strong bonds with metal surfaces and provide long-lasting protection against corrosion. ETHYL 1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLATE is considered an important component in the development of high-performance materials for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 499785-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,9,7,8 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 499785-52:
(8*4)+(7*9)+(6*9)+(5*7)+(4*8)+(3*5)+(2*5)+(1*2)=243
243 % 10 = 3
So 499785-52-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3O2/c1-3-15-10(14)7-4-5-9-8(6-7)11-12-13(9)2/h4-6H,3H2,1-2H3
499785-52-3Relevant articles and documents
The discovery of new scaffold of plant activators: From salicylic acid to benzotriazole
Chang, Kang,Chen, Jian-Qin,Shi, Yan-Xia,Sun, Mei-Jian,Li, Peng-Fei,Zhao, Zhen-Jiang,Zhu, Wei-Ping,Li, Hong-Lin,Xu, Yu-Fang,Li, Bao-Ju,Qian, Xu-Hong
, p. 919 - 926 (2017)
Started from salicylic acid (SA) and related commercialized plant activators, based on molecular three-dimensional shape and pharmacophore similarity comparison (SHAFTS), a new lead compound benzotriazole was predicted and a series of benzotriazole derivatives were designed and synthesized. The bioassay showed that benzotriazole had high activity against a broad spectrum of diseases including fungi and oomycetes in vivo, but no activity in vitro. And the introduction of proper groups at the 1’-position and 5’-position was beneficial to the activity. So, they had the potential to be exploited as novel plant activators.
