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Ethyl 1-(4-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylate is a pyrazole derivative chemical compound with a molecular formula C13H10BrN3O2. It features a bromophenyl group and a cyano group attached to the pyrazole ring, making it a significant building block in the synthesis of pharmaceutical drugs and agrochemicals. ethyl 1-(4-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylate has been investigated for its potential antitumor and antifungal activities, as well as its enzyme-inhibiting capabilities, which contribute to its importance in the development of new compounds with diverse biological and pharmacological applications.

98475-71-9

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98475-71-9 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 1-(4-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylate is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its unique structure and functional groups allow for the development of compounds with potent antitumor and antifungal properties, making it a valuable component in the creation of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, ethyl 1-(4-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylate is utilized as a precursor in the production of agrochemicals. Its ability to inhibit certain enzymes and exhibit antifungal activities contributes to the development of effective crop protection agents, enhancing agricultural productivity and crop yield.
Used in Enzyme Inhibition Research:
Ethyl 1-(4-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylate is employed as a research compound for studying enzyme inhibition. Its potential to modulate enzyme activity makes it a promising candidate for the development of enzyme-targeting drugs, which can be used to treat various diseases and conditions by disrupting specific biochemical pathways.
Used in Drug Discovery and Development:
As a versatile chemical building block, ethyl 1-(4-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylate is used in drug discovery and development processes. Its incorporation into various chemical structures allows for the exploration of new compounds with potential therapeutic benefits, broadening the scope of available treatments for a wide range of medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 98475-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,4,7 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98475-71:
(7*9)+(6*8)+(5*4)+(4*7)+(3*5)+(2*7)+(1*1)=189
189 % 10 = 9
So 98475-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H10BrN3O2/c1-2-19-13(18)11-8-16-17(12(11)7-15)10-5-3-9(14)4-6-10/h3-6,8H,2H2,1H3

98475-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-(4-bromophenyl)-5-cyanopyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 1-(4-BROMOPHENYL)-5-CYANO-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER

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:98475-71-9 SDS

98475-71-9Downstream Products

98475-71-9Relevant academic research and scientific papers

Herbicidal and algicidal 1-aryl-5-cyano-1H-pyrazole-4-carboxamides

-

, (2008/06/13)

The present invention is directed to compounds of the formula STR1 wherein R1 is C1 -C6 alkyl, C5 -C6 cycloalkyl, STR2 each of R2 and R3 is taken separately and is independently

Cyanopyrazole intermediates

-

, (2008/06/13)

5-Cyano-1-substituted-1H-pyrazole-4-carboxylic acids and esters useful as intermediates to the corresponding 4-carboxyamide derivatives having herbicidal and algicidal activity.

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