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5-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLIC ACID is a pyrazole derivative with a molecular formula C11H7N3O4. It features a carboxylic acid functional group and a nitrophenyl group attached to the 5-position of the pyrazole ring. This chemical compound serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals, and it has potential biological activities and medicinal properties. It may also find applications in material science and other industrial fields.

189083-63-4

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189083-63-4 Usage

Uses

Used in Pharmaceutical Synthesis:
5-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its potential to form more complex molecules with therapeutic effects.
Used in Agrochemical Synthesis:
In the agrochemical industry, 5-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLIC ACID is used as a building block for the development of new agrochemicals, contributing to the creation of effective compounds for crop protection and enhancement.
Used in Material Science:
5-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLIC ACID is utilized in material science for its potential to contribute to the development of new materials with specific properties, such as in the creation of advanced polymers or other composites.
Used in Medicinal Research:
In the field of medicinal research, 5-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLIC ACID is studied for its potential biological activities, which may lead to the discovery of new drugs or therapeutic agents.
Used in Industrial Applications:
Beyond its use in pharmaceuticals and agrochemicals, 5-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLIC ACID may have applications in various industrial sectors, where its unique chemical structure can be leveraged for specific purposes, such as in the development of dyes, pigments, or other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 189083-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,0,8 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 189083-63:
(8*1)+(7*8)+(6*9)+(5*0)+(4*8)+(3*3)+(2*6)+(1*3)=174
174 % 10 = 4
So 189083-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H7N3O4/c14-10(15)9-5-8(11-12-9)6-1-3-7(4-2-6)13(16)17/h1-5H,(H,11,12)(H,14,15)

189083-63-4SDS

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 3-(4-nitrophenyl)-1H-pyrazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names TOS-BB-0273

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:189083-63-4 SDS

189083-63-4Downstream Products

189083-63-4Relevant academic research and scientific papers

Synthesis and anti-inflammatory activity of some novel 3-phenyl-N-[3-(4- phenylpiperazin-1yl)propyl]-1H-pyrazole-5-carboxamide derivatives

Nagarapu, Lingaiah,Mateti, Jhansi,Gaikwad, Hanmant K.,Bantu, Rajashaker,Sheeba Rani,Prameela Subhashini

, p. 4138 - 4140 (2011/08/06)

A new series of 3-phenyl-N-[3-(4-phenylpiperazin-1yl)propyl]-1H-pyrazole-5- carboxamide derivatives were synthesized and investigated their anti-inflammatory activities using carrageenan-induced rat paw edema model in vivo. All the synthesized compounds were found to be potent anti-inflammatory agents.

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