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4-Cyclopentenylphenylboronic acid is a chemical compound characterized by the molecular formula C12H13BO2. It features a phenylboronic acid group connected to a cyclopentene ring, which endows it with unique reactivity and selectivity in chemical reactions.

1217501-39-7

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1217501-39-7 Usage

Uses

Used in Organic Synthesis:
4-Cyclopentenylphenylboronic acid is utilized as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds, playing a crucial role in various organic synthesis processes.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-Cyclopentenylphenylboronic acid is employed as a key intermediate in the synthesis of complex organic molecules, contributing to the development of new drugs and therapeutic agents.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
4-Cyclopentenylphenylboronic acid is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it serves as a precursor to create biaryl compounds. Its ability to react selectively and efficiently in these reactions makes it a versatile tool in the synthesis of pharmaceuticals and other specialty chemicals.
Used in Chemical Research:
In the field of chemical research, 4-Cyclopentenylphenylboronic acid is applied as a reagent to explore new synthetic pathways and develop innovative methods for the construction of complex organic structures. Its versatility and selectivity make it an indispensable component in the advancement of chemical science.

Check Digit Verification of cas no

The CAS Registry Mumber 1217501-39-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,5,0 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1217501-39:
(9*1)+(8*2)+(7*1)+(6*7)+(5*5)+(4*0)+(3*1)+(2*3)+(1*9)=117
117 % 10 = 7
So 1217501-39-7 is a valid CAS Registry Number.

1217501-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(cyclopenten-1-yl)phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 4-CYCLOPENTENYLPHENYLBORONIC 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:1217501-39-7 SDS

1217501-39-7Downstream Products

1217501-39-7Relevant academic research and scientific papers

Synthesis method of 4-cyclopentyl biphenyl fluorinated compound

-

, (2018/07/15)

The invention provides a synthesis method of a 4-cyclopentyl biphenyl fluorinated compound. The method comprises the steps of taking p-chloro-halobenzene as a starting material and carrying out Grignard reaction to generate a Grignard reagent II of the p-chloro-halogenated benzene; enabling the generated Grignard reagent II of the p-chloro-halogenated benzene and cyclopentanone to be subjected toa coupling reaction to generate cyclopentanol chlorobenzene; carrying out a dehydration reaction to generate cyclopentene chlorobenzene; carrying out a one-pot reaction to generate 4-cyclopentenyl phenylboronic acid; enabling the generated 4-cyclopentenyl phenylboronic acid and fluorinated halogenated benzene to be subjected to a coupling reaction to generate a 4-cyclopentenyl biphenyl fluorinatedcompound; carrying out a hydrogenation reaction to obtain the 4-cyclopentyl biphenyl fluorinated compound. The synthesis method provided by the invention has the characteristics of being high in conversion rate, low in cost, safe and stable in process, short in reaction steps, environmentally friendly in process route, and less in pollutant emission.

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