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23814-12-2

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23814-12-2 Usage

Description

Benzotriazole-5-carboxylic acid, with the CAS number 23814-12-2, is an earthy yellow powder that serves as a useful research chemical. It is known for its chemical properties and potential applications in various fields.

Uses

Used in Research and Development:
Benzotriazole-5-carboxylic acid is used as a research chemical for the development and study of diverse dimensional coordination assemblies and coordination polymers. It plays a crucial role in the synthesis process, contributing to the formation of complex structures with potential applications in various industries.
Used in Coordination Chemistry:
Benzotriazole-5-carboxylic acid is used as a bifunctional ligand in the solvent-induced synthesis of diverse dimensional coordination assemblies of cupric benzotriazole-5-carboxylate. This application highlights its importance in the field of coordination chemistry, where it helps create complex structures with unique properties.
Used in Hydrothermal Synthesis:
In the hydrothermal synthesis of new coordination polymers, such as [Zn(Btca)(Phen)]n (H2Btca = benzotriazole-5-carboxylic acid, Phen = 1,10-phenanthroline), benzotriazole-5-carboxylic acid is utilized as a key component. This application demonstrates its versatility and potential in creating novel materials with specific properties for various applications.
Overall, benzotriazole-5-carboxylic acid is a versatile chemical with a wide range of applications in research, coordination chemistry, and hydrothermal synthesis, making it a valuable asset in the development of new materials and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 23814-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,1 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23814-12:
(7*2)+(6*3)+(5*8)+(4*1)+(3*4)+(2*1)+(1*2)=92
92 % 10 = 2
So 23814-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5N3O2/c11-7(12)4-1-2-5-6(3-4)9-10-8-5/h1-3H,(H,11,12)(H,8,9,10)

23814-12-2 Well-known Company Product Price

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  • Aldrich

  • (304239)  Benzotriazole-5-carboxylicacid  99%

  • 23814-12-2

  • 304239-5G

  • 601.38CNY

  • Detail
  • Aldrich

  • (304239)  Benzotriazole-5-carboxylicacid  99%

  • 23814-12-2

  • 304239-25G

  • 2,059.20CNY

  • Detail

23814-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2H-benzotriazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names Benzotriazole-5-carboxylic acid

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:23814-12-2 SDS

23814-12-2Relevant articles and documents

INDAZOLES AS LRRK2 INHIBITORS

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Page/Page column 99, (2020/10/09)

The present invention is directed to indazole compounds which are inhibitors of LRRK2 and are useful in the treatment of CNS 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.

Compound and use

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, (2008/06/13)

A compound contains a ligand group and at least one group of the general formula --XRn where X is a linking group which contains at least one hetero-atom, R is a saturated hydrocarbyl group containing at least six carbon atoms or is an unsaturated hydrocarbyl group containing at least three carbon atoms. The ligand group can be a polyhydroxyhydrocarbyl, a triazole, an imidazole, an indazole, a thiazole, an oxazole, a carbamate, an xanthate or a phthalazine. The compounds can be used to improve bonding between a metal and a coating material in contact with the metal surface. The metal may be a tire cord and the coating material rubber or a rubber composition.

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