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5-(2-Bromo-5-fluoro-phenyl)-1-tert-butyl-4-iodo-1H-pyrazole is a pyrazole derivative with the molecular formula C13H13BrF2IN2. It is a chemical compound known for its diverse pharmacological properties and potential as a potent enzyme inhibitor, making it a promising candidate for the development of new drugs to treat various diseases. Its unique chemical structure and properties position it for further research and development in medicinal chemistry and drug discovery.

1245643-25-7

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1245643-25-7 Usage

Uses

Used in Pharmaceutical Industry:
5-(2-Bromo-5-fluoro-phenyl)-1-tert-butyl-4-iodo-1H-pyrazole is used as a potent enzyme inhibitor for the development of new drugs to treat various diseases. Its ability to inhibit specific enzymes makes it a valuable compound in the search for novel therapeutic agents.
Used in Medicinal Chemistry Research:
This pyrazole derivative is used as a key compound in medicinal chemistry research to explore its potential applications in drug discovery. Its unique chemical structure and properties provide a foundation for further investigation into its pharmacological effects and mechanisms of action.
Used in Drug Development:
5-(2-Bromo-5-fluoro-phenyl)-1-tert-butyl-4-iodo-1H-pyrazole is utilized in drug development as a starting point for the synthesis of new compounds with improved pharmacological properties. Its structure can be modified to create derivatives with enhanced potency, selectivity, and reduced side effects.
Used in Drug Screening:
5-(2-Bromo-5-fluoro-phenyl)-1-tert-butyl-4-iodo-1H-pyrazole is employed in drug screening processes to identify potential lead candidates for further optimization and development. Its diverse pharmacological properties make it a valuable tool in the search for new therapeutic agents with novel mechanisms of action.
Used in Chemical Synthesis:
5-(2-Bromo-5-fluoro-phenyl)-1-tert-butyl-4-iodo-1H-pyrazole serves as a versatile building block in chemical synthesis, allowing for the creation of a wide range of pyrazole-based compounds with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1245643-25-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,6,4 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1245643-25:
(9*1)+(8*2)+(7*4)+(6*5)+(5*6)+(4*4)+(3*3)+(2*2)+(1*5)=147
147 % 10 = 7
So 1245643-25-7 is a valid CAS Registry Number.

1245643-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-bromo-5-fluorophenyl)-1-tert-butyl-4-iodopyrazole

1.2 Other means of identification

Product number -
Other names 5-(2-Bromo-5-fluorophenyl)-1-(tert-butyl)-4-iodo-1H-pyrazole

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:1245643-25-7 SDS

1245643-25-7Relevant academic research and scientific papers

PROCESS FOR THE PRODUCTION OF FUSED, TRICYCLIC SULFONAMIDES

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Page/Page column 100-101, (2010/11/04)

The present invention provides methods, i.e., scalable or large-scale processes for the production of fused, tricyclic sulfonamido analogs, such as substituted or unsubstituted 5- (aryl-sulfonyl)-4,5-dihydro- 1H-pyrazolo[4,3-c]quinolines and 5-(heteroaryl-sulfonyl)-4,5- dihydro-1H-pyrazolo[4,3-c]quinolines. Exemplary methods of the invention include an intra-molecular cyclization step, in which a carbon-nitrogen bond is formed, and which employs a copper-based catalyst that contains at least one organic ligand, such as DMEDA. The invention further provides compounds, which are useful as intermediates in the methods of the invention.

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