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1H-Benzotriazole-4-carboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120723-06-0

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120723-06-0 Usage

Use as a corrosion inhibitor

Effective in protecting metal surfaces in aqueous systems

Industrial applications

Valued in industries such as automotive, aerospace, and electronics

Stabilizer for polymers

Prevents degradation due to UV radiation and oxidation

Versatility and effectiveness

Makes it a valuable chemical in various industrial and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 120723-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,7,2 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 120723-06:
(8*1)+(7*2)+(6*0)+(5*7)+(4*2)+(3*3)+(2*0)+(1*6)=80
80 % 10 = 0
So 120723-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O2/c1-13-8(12)5-3-2-4-6-7(5)10-11-9-6/h2-4H,1H3,(H,9,10,11)

120723-06-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2H-benzotriazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 1H-1,2,3-benzotriazole-7-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:120723-06-0 SDS

120723-06-0Relevant academic research and scientific papers

CYCLIC DINUCLEOTIDES AS ANTICANCER AGENTS

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Page/Page column 87, (2019/03/17)

The present invention is directed to compounds of the formula (I) wherein all substituents are defined herein, as well as pharmaceutically acceptable compositions comprising compounds of the invention and methods of using said compositions in the treatment of various disorders.

CYCLIC DINUCLEOTIDES AS ANTICANCER AGENTS

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Paragraph 1450; 1465; 1466, (2019/02/13)

The present invention is directed to compounds of the formulae I, II and III as shown below wherein all substituents are defined herein, as well as pharmaceutically acceptable compositions comprising compounds of the invention and methods of using said compositions in the treatment of various disorders.

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 (2017/05/16)

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.

SUBSTITUTED DIHYDROPYRIDINES AND METHODS OF USE

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Page/Page column 132-133, (2010/11/27)

Compounds are provided that are modulators of the C5a receptor. The compounds are substituted dihydropyridines and are useful in pharmaceutical compositions, methods for the treatment of diseases and disorders involving the pathologic activtation of C5a receptors.

AMIDE SUBSTITUTED INDAZOLE AND BENZOTRIAZOLE DERIVATIVES AS POLY(ADP-RIBOSE)POLYMERASE (PARP) INHIBITORS

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Page/Page column 85, (2008/06/13)

The present invention relates to compounds of formula (I) and pharmaceutically acceptable salts or tautomers thereof which are inhibitors of poly (ADP-ribose) polymerase (PARP) and thus useful for the treatment of cancer, inflammatory diseases, reperfusio

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