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4-chloro-1-(difluoromethyl)-1H-pyrazole-3-carboxylic acid is a chemical compound characterized by the molecular formula C5H3ClF2N2O2. It features a 4-chloro-1H-pyrazole-3-carboxylic acid core with a difluoromethyl group at the 1-position, making it a carboxylic acid derivative. 4-chloro-1-(difluoromethyl)-1H-pyrazole-3-carboxylic acid serves as a synthetic building block for the creation of various biologically active molecules and agrochemicals, and it is recognized for its inhibitory effect on the enzyme Inosine 5’-monophosphate dehydrogenase, which is vital in the biosynthesis of guanine nucleotides.

1310350-99-2

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1310350-99-2 Usage

Uses

Used in Pharmaceutical Industry:
4-chloro-1-(difluoromethyl)-1H-pyrazole-3-carboxylic acid is utilized as a synthetic intermediate for the development of pharmaceuticals. Its role in the synthesis of biologically active compounds makes it a valuable component in the creation of new drugs with potential therapeutic applications.
Used in Agricultural Industry:
In the agricultural sector, 4-chloro-1-(difluoromethyl)-1H-pyrazole-3-carboxylic acid is employed as a precursor in the synthesis of agrochemicals. Its ability to form various active compounds contributes to the development of new pesticides or other agricultural chemicals aimed at enhancing crop protection and yield.
Used as an Enzyme Inhibitor:
4-chloro-1-(difluoromethyl)-1H-pyrazole-3-carboxylic acid is used as a potent inhibitor of the enzyme Inosine 5’-monophosphate dehydrogenase. This application is significant in research and development for understanding the enzyme's role in guanine nucleotide biosynthesis and exploring the compound's potential as a therapeutic agent in conditions related to nucleotide metabolism.
Further research is being conducted to delve deeper into the properties and potential uses of 4-chloro-1-(difluoromethyl)-1H-pyrazole-3-carboxylic acid, indicating its importance in both scientific inquiry and practical applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1310350-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,3,5 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1310350-99:
(9*1)+(8*3)+(7*1)+(6*0)+(5*3)+(4*5)+(3*0)+(2*9)+(1*9)=102
102 % 10 = 2
So 1310350-99-2 is a valid CAS Registry Number.

1310350-99-2Relevant articles and documents

2-AMINO-6-METHYL-4,4a,5,6-TETRAHYDROPYRANO[3,4-d][1,3]THIAZIN-8a(8H)-YL-1,3-THIAZOL-4-YL AMIDES

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Page/Page column 77; 81; 82, (2015/11/17)

The present invention is directed to compounds, tautomers and pharmaceutically acceptable salts of the compounds which are disclosed, wherein the compounds have the structure of Formula (I), and the variable R1 is as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

β-secretase (BACE1) inhibitors with high in vivo efficacy suitable for clinical evaluation in Alzheimer's disease

Hilpert, Hans,Guba, Wolfgang,Woltering, Thomas J.,Wostl, Wolfgang,Pinard, Emmanuel,Mauser, Harald,Mayweg, Alexander V.,Rogers-Evans, Mark,Humm, Roland,Krummenacher, Daniela,Muser, Thorsten,Schnider, Christian,Jacobsen, Helmut,Ozmen, Laurence,Bergadano, Alessandra,Banner, David W.,Hochstrasser, Remo,Kuglstatter, Andreas,David-Pierson, Pascale,Fischer, Holger,Polara, Alessandra,Narquizian, Robert

, p. 3980 - 3995 (2013/06/27)

An extensive fluorine scan of 1,3-oxazines revealed the power of fluorine(s) to lower the pKa and thereby dramatically change the pharmacological profile of this class of BACE1 inhibitors. The CF3 substituted oxazine 89, a potent and

1,4 OXAZINES AS BACE1 AND/OR BACE2 INHIBITORS

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, (2012/07/28)

The present invention relates to 1,4 Oxazines of formula I having BACE 1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the prese

1,4,5,6-TETRAHYDRO-PYRIMIDIN-2-YLAMINE COMPOUNDS

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, (2012/02/15)

This invention relates to compounds of the formula wherein R1 to R9 are as described below, or to pharmaceutically acceptable salts thereof. These compounds are BACE2 inhibitors and can be used as medicaments for the therapeutic and/

1,4,5,6-TETRAHYDRO-PYRIMIDIN-2-YLAMINE COMPOUNDS

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, (2012/03/09)

This invention relates to compounds of the formula wherein R1 to R9 are as described below, or to pharmaceutically acceptable salts thereof. These compounds are BACE2 inhibitors and can be used as medicaments for the therapeutic and/

1,4 OXAZINES AS BACE1 AND/OR BACE2 INHIBITORS

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, (2012/08/07)

The present invention relates to 1,4 Oxazines of formula (I): having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the pre

1,4-OXAZEPINES AS BACE1 AND/OR BACE2 INHIBITORS

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, (2012/09/25)

The present invention relates to 1,4-Oxazepines of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the pres

1,4-OXAZEPINES AS BACE1 AND/OR BACE2 INHIBITORS

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, (2012/10/08)

The present invention relates to 1,4-Oxazepines of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the pres

1,3-OXAZINES AS BACE 1 AND/OR BACE2 INHIBITORS

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, (2012/12/13)

The present invention provides compounds of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present inv

1,3-OXAZINES AS BACE1 AND/OR BACE2 INHIBITORS

-

, (2012/12/13)

The present invention provides compounds of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present inv

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