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77169-11-0

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77169-11-0 Usage

Description

3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is a chemical compound with the molecular formula C11H10N2O2, belonging to the class of carboxylic acids and is a derivative of pyrazole. It is used in organic synthesis and pharmaceutical research, particularly in the development of potential drug candidates. 3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID has been studied for its potential biological activities, including anti-inflammatory, antimicrobial, and antifungal properties, making it a promising building block for the development of new drugs and materials.

Uses

Used in Pharmaceutical Research:
3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceutical compounds for the development of potential drug candidates.
Used in Organic Synthesis:
3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is used as a building block in the synthesis of new organic compounds and materials.
Used in Anti-Inflammatory Applications:
3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is used as an anti-inflammatory agent for the development of potential therapeutic agents to treat inflammation-related conditions.
Used in Antimicrobial Applications:
3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is used as an antimicrobial agent for the development of potential therapeutic agents to treat microbial infections.
Used in Antifungal Applications:
3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is used as an antifungal agent for the development of potential therapeutic agents to treat fungal infections.

Check Digit Verification of cas no

The CAS Registry Mumber 77169-11-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,6 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77169-11:
(7*7)+(6*7)+(5*1)+(4*6)+(3*9)+(2*1)+(1*1)=150
150 % 10 = 0
So 77169-11-0 is a valid CAS Registry Number.

77169-11-0SDS

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 3-methyl-1-phenylpyrazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names acide methyl-3 phenyl-1 pyrazolecarboxylique-4

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:77169-11-0 SDS

77169-11-0Relevant articles and documents

AMIDE COMPOUNDS AND MEDICINAL USE THEREOF

-

Page 44, (2010/01/31)

The present invention relates to a compound of the formula wherein R1 is substituted aryl, heteroaryl and the like, R2 and R3 are hydrogen, alkyl, halogen, hydroxyl group and the like, Q is N, CH and the like, W is hydrogen, alkyl, hydroxycarbonylalkyl and the like, X is halogen, cyano, nitro, amino and the like, X' is hydrogen, halogen, cyano, nitro, and Y is alkyl, hydroxyl group, alkoxy, mercapto and the like and a salt thereof, and a medicine containing the said compound. The compound of the present invention shows a superior inhibitory effect on activated lymphocytes proliferation and is useful as an agent for the prophylaxis or treatment of various autoimmune diseases.

CONVERSION DE L'ACETYL-5 URACILE EN DERIVES PYRAZOLIQUES PAR L'HYDRAZINE ET LES HYDRAZINES MONOSUBSTITUEES

Bajnati, Abdelilah,Hubert-Habart, Michel

, p. 540 - 547 (2007/10/02)

5-Acetyl uracile 1 is easily transformed by hydrazine and methylhydrazine into 4-allophanoyl-3-methyl pyrazole 2 (R=H) and 4-allophanoyl-1,3-dimethyl pyrazole 2 (R=CH3).The pyrazoles 2, in boiling butanol and in the presence of hydrochloric acid lead resp

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