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(3,5-DIMETHYL-1H-PYRAZOL-4-YL)ACETIC ACID is a chemical compound characterized by the molecular formula C9H12N2O2. It is a pyrazole derivative featuring methyl groups at the 3 and 5 positions on the pyrazole ring, with an acetic acid group attached to the ring. (3,5-DIMETHYL-1H-PYRAZOL-4-YL)ACETIC ACID is recognized for its potential therapeutic properties and is frequently utilized in pharmaceutical research and drug development.

32701-75-0

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32701-75-0 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
(3,5-DIMETHYL-1H-PYRAZOL-4-YL)ACETIC ACID is employed as a key component in the discovery and development of new pharmaceuticals due to its potential therapeutic properties. Its unique structure allows it to interact with various biological targets, offering a wide range of applications in treating different conditions.
Used in the Treatment of Various Conditions:
While further research is necessary to fully understand its potential uses and mechanisms of action, (3,5-DIMETHYL-1H-PYRAZOL-4-YL)ACETIC ACID may have applications in the treatment of a variety of conditions. Its presence in pharmaceutical research suggests that it could be a promising candidate for addressing unmet medical needs.

Check Digit Verification of cas no

The CAS Registry Mumber 32701-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,0 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32701-75:
(7*3)+(6*2)+(5*7)+(4*0)+(3*1)+(2*7)+(1*5)=90
90 % 10 = 0
So 32701-75-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O2/c1-4-6(3-7(10)11)5(2)9-8-4/h3H2,1-2H3,(H,8,9)(H,10,11)

32701-75-0SDS

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 2-(3,5-dimethyl-1H-pyrazol-4-yl)acetic 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:32701-75-0 SDS

32701-75-0Downstream Products

32701-75-0Relevant academic research and scientific papers

Design and synthesis of high affinity inhibitors of Plasmodium falciparum and Plasmodium vivax N-myristoyltransferases directed by ligand efficiency dependent lipophilicity (LELP)

Rackham, Mark D.,Brannigan, James A.,Rangachari, Kaveri,Meister, Stephan,Wilkinson, Anthony J.,Holder, Anthony A.,Leatherbarrow, Robin J.,Tate, Edward W.

, p. 2773 - 2788 (2014/04/17)

N-Myristoyltransferase (NMT) is an essential eukaryotic enzyme and an attractive drug target in parasitic infections such as malaria. We have previously reported that 2-(3-(piperidin-4-yloxy)benzo[b]thiophen-2-yl)-5-((1,3, 5-trimethyl-1H-pyrazol-4-yl)meth

NOVEL COMPOUNDS AND THEIR USE IN THERAPY

-

, (2013/06/27)

The invention provides compounds which inhibit N-myristoyltransferase and are selective for protozoal N-myristoyltransferase and, consequently suitable to treat microbial infections, including viral and fungal infections, and protozoan infections such as malaria, leishmaniasis and sleeping sickness.

Pyrazol-4-acetic acid compounds

-

, (2008/06/13)

Pyrazol-4-acetic acid compounds, such as substituted pyrazol-4-acetic acid, its esters, amides, nitriles and their pharamaceutically acceptable salts and method for the preparation of these compounds are disclosed. The novel compounds are useful analgesics, anti-inflammatory, and antipyretics.

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