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2-Formyl-4-(trifluoromethyl)phenylboronic acid is a chemical compound that belongs to the boronic acids category. It is characterized by the presence of a 2-Formyl group, which imparts aldehyde functionality, and a 4-(trifluoromethyl) group, which enhances its reactivity due to the inductive effect of the fluorine atoms. 2-Formyl-4-(trifluoromethyl)phenylboronic acid is predominantly utilized in scientific research, particularly within the realms of organic and medicinal chemistry, where it serves as a reactant or ligand in a variety of chemical reactions.

1217501-35-3

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1217501-35-3 Usage

Uses

Used in Organic Chemistry:
2-Formyl-4-(trifluoromethyl)phenylboronic acid is used as a reactant in various organic synthesis processes. Its aldehyde functionality and trifluoromethyl group enable it to participate in a range of reactions, making it a valuable building block for the creation of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-Formyl-4-(trifluoromethyl)phenylboronic acid is employed as a reactant or ligand in the synthesis of pharmaceutical compounds. Its unique structural features allow it to be incorporated into drug molecules, potentially leading to the development of new therapeutic agents.
Used in Suzuki-Miyaura Coupling:
2-Formyl-4-(trifluoromethyl)phenylboronic acid is used as a reactant in Suzuki-Miyaura coupling reactions, a widely recognized method for forming carbon-carbon bonds. This cross-coupling reaction is instrumental in the production of pharmaceuticals and various fine chemicals, as it allows for the efficient construction of complex molecular structures.
Used in Pharmaceutical Production:
2-Formyl-4-(trifluoromethyl)phenylboronic acid is used as a key intermediate in the synthesis of pharmaceutical compounds. Its involvement in various chemical reactions, such as Suzuki-Miyaura coupling, contributes to the development of new drugs and the improvement of existing ones, ultimately benefiting the healthcare industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1217501-35-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,5,0 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1217501-35:
(9*1)+(8*2)+(7*1)+(6*7)+(5*5)+(4*0)+(3*1)+(2*3)+(1*5)=113
113 % 10 = 3
So 1217501-35-3 is a valid CAS Registry Number.

1217501-35-3SDS

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-Formyl-4-(trifluoromethyl)phenylboronic acid

1.2 Other means of identification

Product number -
Other names [2-formyl-4-(trifluoromethyl)phenyl]boronic acid

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:1217501-35-3 SDS

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