499785-52-3 Usage
Description
ETHYL 1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLATE is a chemical compound belonging to the benzotriazole family, known for its corrosion inhibition and metal surface protection properties. Characterized by its ethyl and carboxylate functional groups, this compound forms strong bonds with metal surfaces, offering long-lasting protection against corrosion. It plays a significant role in the development of high-performance materials for various industrial applications.
Uses
Used in Industrial Water Treatment:
ETHYL 1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLATE is used as a corrosion inhibitor to protect metal surfaces from degradation in industrial water treatment processes. Its ability to form strong bonds with metal surfaces helps in providing long-lasting protection against corrosion.
Used in Polymer and Coating Production:
In the production of polymers and coatings, ETHYL 1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLATE serves as a stabilizer. Its presence enhances the stability and performance of the final products, contributing to their durability and resistance to environmental factors.
Used in High-Performance Material Development:
ETHYL 1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLATE is used as an important component in the development of high-performance materials for various industrial applications. Its unique properties, such as corrosion inhibition and metal surface protection, make it a valuable addition to the formulation of advanced materials with improved performance characteristics.
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.