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133902-66-6

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133902-66-6 Usage

General Description

"[1-(4-Chlorophenyl)-1H-1,2,3-triazol-4-yl]methanol" is a specialized chemical compound that belongs to the group of 1,2,3-triazoles. 1,2,3-triazole structures are often found in pharmaceutical compounds due to their versatile biological activities. The prefix "1-(4-Chlorophenyl)" in the chemical's name indicates the presence of a chlorophenyl group attached to the 1-position of the triazole ring. On the other side, the "4-yl]methanol" indicates a methanol group attached to the 4-position. The exact attributes, reactivity, and applications of this chemical can vary widely depending on the broader context of its use, however, it generally possesses both the typical reactivity of a 1,2,3-triazole, and the typical properties associated with a chlorophenyl group and a methanol group.

Check Digit Verification of cas no

The CAS Registry Mumber 133902-66-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,0 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133902-66:
(8*1)+(7*3)+(6*3)+(5*9)+(4*0)+(3*2)+(2*6)+(1*6)=116
116 % 10 = 6
So 133902-66-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClN3O/c10-7-1-3-9(4-2-7)13-5-8(6-14)11-12-13/h1-5,14H,6H2

133902-66-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H64737)  1-(4-Chlorophenyl)-1H-1,2,3-triazole-4-methanol, 98%   

  • 133902-66-6

  • 250mg

  • 196.0CNY

  • Detail
  • Alfa Aesar

  • (H64737)  1-(4-Chlorophenyl)-1H-1,2,3-triazole-4-methanol, 98%   

  • 133902-66-6

  • 1g

  • 491.0CNY

  • Detail
  • Alfa Aesar

  • (H64737)  1-(4-Chlorophenyl)-1H-1,2,3-triazole-4-methanol, 98%   

  • 133902-66-6

  • 5g

  • 1960.0CNY

  • Detail

133902-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(4-Chlorophenyl)-1H-1,2,3-triazol-4-yl]methanol

1.2 Other means of identification

Product number -
Other names [1-(4-chlorophenyl)triazol-4-yl]methanol

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:133902-66-6 SDS

133902-66-6Relevant articles and documents

Anti-Lung Cancer Activities of 1,2,3-Triazole Curcumin Derivatives via Regulation of the MAPK/NF-κB/STAT3 Signaling Pathways

Zhi, Tai Xin,Liu, Kai Qiang,Cai, Kun Yi,Zhao, Yu Chao,Li, Zhen Wang,Wang, Xin,He, Xin Hua,Sun, Xian Yu

, (2021/12/01)

In this study, a series of curcumin derivatives containing 1,2,3-triazole were designed and synthesized, and their inhibitory activities against the proliferation of lung cancer cells were studied. Compound 5 k (3,4-dichlorobenzyltriazole methyl curcumin)

Design, synthesis and effect of triazole derivatives against some toxic activities of Bothrops jararaca venom

da Silva, Aldo R.,da Silva, Ana Cláudia R.,Donza, Marcio Roberto H.,de Aquino, Gabriel Alves S.,Kaiser, Carlos R.,Sanchez, Eladio F.,Ferreira, Sabrina B.,Fuly, André L.

, p. 182 - 195 (2020/10/26)

According to the World Health Organization, snakebite envenoming is a neglected disease that affects around 5.4 million people worldwide each year. In Brazil, in 2019 there were 29,000 cases of accidents, with 104 deaths. The genus Bothrops was responsibl

[Et3NH][HSO4] catalyzed solvent-free synthesis of new 1,2,3-triazolidene-indolinone derivatives

Nagargoje, Amol A.,Pisal, Parshuram M.,Raza, Akram K.,Shingate, Bapurao B.,Siddiqui, Madiha M.

, (2022/02/03)

A series of new 1,2,3-triazolidene-indolinone derivatives (17a-j) were designed and synthesized via [Et3NH] [HSO4] catalyzed solvent-free approach. The synthesis strongly relied on Knoevenagel condensation of 1,4-disubstituted 1,2,3-

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