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138907-79-6

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138907-79-6 Usage

General Description

1-(4-Methoxyphenyl)-1H-pyrazole-4-carboxylic acid is a chemical compound with the molecular formula C11H10N2O3. It is a pyrazole derivative, characterized by a pyrazole core substituted with a 4-methoxyphenyl group and a carboxylic acid functionality. 1-(4-Methoxyphenyl)-1H-pyrazole-4-carboxylic acid has potential applications in the field of medicinal chemistry and drug development due to its ability to modulate biological processes. It may also have uses in the synthesis of other organic compounds. The specific properties and potential uses of this chemical may vary depending on the context and intended application.

Check Digit Verification of cas no

The CAS Registry Mumber 138907-79-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,0 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138907-79:
(8*1)+(7*3)+(6*8)+(5*9)+(4*0)+(3*7)+(2*7)+(1*9)=166
166 % 10 = 6
So 138907-79-6 is a valid CAS Registry Number.

138907-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methoxyphenyl)pyrazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:138907-79-6 SDS

138907-79-6Downstream Products

138907-79-6Relevant articles and documents

Synthesis of pyrazole-carboxamides and pyrazole-carboxylic acids derivatives: Simple methods to access powerful building blocks

Ferreira, Byanca Silva,Silva, Rafaela Corrêa,Souto, Bernardo Araújo,Dos Santos, Maurício Silva

, p. 335 - 343 (2021/09/07)

Hybrid systems containing pyrazole moiety show a wide spectrum of biological activities. To access novel hybrids with pyrazole ring, in this work we synthesized twenty pyrazole-carboxylic acids and twenty pyrazole-carboxamides, using simple synthetic methods, to be used as building blocks in the development of new structures.

COMPOSITIONS AND METHODS FOR TREATING CANCER

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Paragraph 0746; 0747, (2018/09/11)

Disclosed herein, inter alia, are compositions and methods for modulating Ras and treating cancer.

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.

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