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(5-fluoro-2-(pyrrolidin-1-ylMethyl)phenyl)boronic acid is a chemical compound that features a boronic acid group attached to a fluorinated phenyl ring with a pyrrolidin-1-ylMethyl substituent. (5-fluoro-2-(pyrrolidin-1-ylMethyl)phenyl)boronic acid is recognized for its role in organic synthesis and medicinal chemistry, where it serves as a versatile building block for the creation of biologically active molecules. The unique structure, which includes a fluorine atom and a pyrrolidin-1-ylMethyl group, endows the compound with distinctive chemical properties and potential for further modification, making it a valuable asset in pharmaceutical research and drug development.

1333121-77-9

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1333121-77-9 Usage

Uses

Used in Organic Synthesis:
(5-fluoro-2-(pyrrolidin-1-ylMethyl)phenyl)boronic acid is utilized as a key building block in organic synthesis for the construction of complex organic molecules. Its unique structure allows for a variety of chemical reactions, facilitating the synthesis of new compounds with potential applications in various fields.
Used in Medicinal Chemistry:
In the realm of medicinal chemistry, (5-fluoro-2-(pyrrolidin-1-ylMethyl)phenyl)boronic acid is employed as a precursor to develop biologically active molecules. The presence of the fluorine and pyrrolidin-1-ylMethyl groups provides opportunities for chemical modification, which can enhance the pharmacological properties of the resulting molecules, making them more effective in treating diseases.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
(5-fluoro-2-(pyrrolidin-1-ylMethyl)phenyl)boronic acid is used as a reactant in Suzuki-Miyaura cross-coupling reactions, a widely employed method in organic chemistry for the formation of carbon-carbon bonds. Boronic acids, including this specific compound, are known for their ability to form stable complexes with diols, which is crucial for the success of these coupling reactions.
Used in Drug Discovery and Development:
(5-fluoro-2-(pyrrolidin-1-ylMethyl)phenyl)boronic acid is an important tool in drug discovery and development due to its potential to be modified and incorporated into new pharmaceutical compounds. Its unique structural features and reactivity make it a promising candidate for the design of novel drugs with improved efficacy and selectivity.
Used in Chemical Research:
In the field of chemical research, (5-fluoro-2-(pyrrolidin-1-ylMethyl)phenyl)boronic acid is used to explore new reaction mechanisms, study the effects of structural modifications on chemical and biological properties, and develop new synthetic methodologies. Its versatility and the potential for modification make it an invaluable compound for advancing knowledge in chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1333121-77-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,1,2 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1333121-77:
(9*1)+(8*3)+(7*3)+(6*3)+(5*1)+(4*2)+(3*1)+(2*7)+(1*7)=109
109 % 10 = 9
So 1333121-77-9 is a valid CAS Registry Number.

1333121-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-fluoro-2-(pyrrolidin-1-ylmethyl)phenyl)boronic 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

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More Details:1333121-77-9 SDS

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