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1-[3-CYANO-4-(2,2-DIMETHYL-PROPOXY)-PHENYL]-1H-PYRAZOLE-4-CARBOXYLIC ACID is a chemical compound with potential pharmaceutical applications. It features a pyrazole ring with a carboxylic acid group and a cyano group, along with a 2,2-dimethylpropoxy side chain. 1-[3-CYANO-4-(2,2-DIMETHYL-PROPOXY)-PHENYL]-1H-PYRAZOLE-4-CARBOXYLIC ACID's structural features may confer biological activity, making it a candidate for drug development across various therapeutic areas. Further research is necessary to explore its properties and possible applications comprehensively.

206884-98-2

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206884-98-2 Usage

Uses

Used in Pharmaceutical Development:
1-[3-CYANO-4-(2,2-DIMETHYL-PROPOXY)-PHENYL]-1H-PYRAZOLE-4-CARBOXYLIC ACID is used as a chemical intermediate for the development of pharmaceuticals due to its unique structural components that may contribute to its biological activity.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1-[3-CYANO-4-(2,2-DIMETHYL-PROPOXY)-PHENYL]-1H-PYRAZOLE-4-CARBOXYLIC ACID serves as a compound of interest for studying its potential interactions with biological targets, which could lead to the creation of new drugs.
Used in Drug Discovery:
1-[3-CYANO-4-(2,2-DIMETHYL-PROPOXY)-PHENYL]-1H-PYRAZOLE-4-CARBOXYLIC ACID is utilized in drug discovery processes to identify its potential as a lead compound for treating various diseases, given its distinct chemical structure.

Check Digit Verification of cas no

The CAS Registry Mumber 206884-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,8,8 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 206884-98:
(8*2)+(7*0)+(6*6)+(5*8)+(4*8)+(3*4)+(2*9)+(1*8)=162
162 % 10 = 2
So 206884-98-2 is a valid CAS Registry Number.

206884-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-cyano-4-(2,2-dimethylpropoxy)phenyl]pyrazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names niraxostat

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:206884-98-2 SDS

206884-98-2Downstream Products

206884-98-2Relevant academic research and scientific papers

Synthesis and bioevaluation of 1-phenyl-pyrazole-4-carboxylic acid derivatives as potent xanthine oxidoreductase inhibitors

Li, Jing,Wu, Fangping,Liu, Xingguo,Zou, Yake,Chen, Huixiong,Li, Zheng,Zhang, Lei

, p. 20 - 30 (2017/09/19)

A diverse library of 1-phenyl-pyrazole-4-carboxylic acid derivatives were synthesized and evaluated for their inhibitory potency against xanthine oxidoreductase (XOR) in vitro and vivo, and the structure-activity relationship (SAR) analyses were also pres

Synthesis and structure - Activity relationships of 1-phenylpyrazoles as xanthine oxidase inhibitors

Ishibuchi, Seigo,Morimoto, Hiroshi,Oe, Takanori,Ikebe, Tsuguo,Inoue, Hiroyoshi,Fukunari, Atsushi,Kamezawa, Miho,Yamada, Ichimaro,Naka, Yoichi

, p. 879 - 882 (2007/10/03)

A series of 1-phenylpyrazoles was evaluated for inhibitory activity against xanthine oxidase in vitro. Of the compounds prepared, 1-(3-cyano-4-neopentyloxyphenyl)pyrazole-4-carboxylic acid (Y-700) had the most potent enzyme inhibition and displayed longer-lasting hypouricemic action than did allopurinol in a rat model of hyperuricemia induced by the uricase inhibitor potassium oxonate.

1-phenylpyrazole compounds and medicinal application thereof

-

, (2008/06/13)

PCT No. PCT/JP97/03840 Sec. 371 Date Sep. 22, 1998 Sec. 102(e) Date Sep. 22, 1998 PCT Filed Oct. 22, 1997 PCT Pub. No. WO98/18765 PCT Pub. Date May 7, 19981-Phenylpyrazole compounds of the formula (1): which is exemplified by 5-amino-1-(3-cyano-4-isobutoxyphenyl)pyrazole-4-carboxylic acid, an optical isomer thereof and a pharmaceutically acceptable salt thereof. These compounds have a xanthine oxidase inhibitory activity and are useful as therapeutic agents for diseases such as hyperuricacidemia and gout.

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