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2-Benzyloxy-3-fluorophenylboronic acid is an aryl boronic acid derivative featuring a benzyl ether substituent at the 2-position and a fluorine atom at the 3-position of the phenyl ring. It is a significant chemical compound utilized in organic synthesis and pharmaceutical research, known for its role as a building block in creating biologically active molecules, including pharmaceutical drugs and agrochemicals.

1256355-53-9

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1256355-53-9 Usage

Uses

Used in Pharmaceutical Research and Development:
2-Benzyloxy-3-fluorophenylboronic acid serves as a key building block in the synthesis of various pharmaceutical drugs. Its boronic acid functionality is particularly valuable for Suzuki-Miyaura cross-coupling reactions, which facilitate the formation of carbon-carbon bonds essential for constructing complex molecular structures.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Benzyloxy-3-fluorophenylboronic acid is employed as a versatile reagent for the creation of a wide range of organic compounds. Its unique structural features, including the benzyl ether and fluorine substituents, allow for the development of molecules with specific properties and reactivity.
Used in Agrochemical Development:
2-Benzyloxy-3-fluorophenylboronic acid also finds application in the agrochemical industry, where it is used in the synthesis of biologically active molecules with potential pesticidal or herbicidal properties. Its ability to form carbon-carbon bonds through cross-coupling reactions contributes to the design of novel and effective agrochemicals.
Used in Medicinal Chemistry:
In medicinal chemistry, 2-Benzyloxy-3-fluorophenylboronic acid is utilized for the development of new therapeutic agents. Its fluorine substituent can impart specific properties to the target compounds, such as enhanced metabolic stability or improved pharmacokinetics, making it a valuable component in the design of innovative drugs.
Overall, 2-Benzyloxy-3-fluorophenylboronic acid is an important chemical reagent with diverse applications across various industries, including pharmaceuticals, agrochemicals, and material chemistry, due to its unique structural features and reactivity in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1256355-53-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1256355-53:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*5)+(2*5)+(1*3)=159
159 % 10 = 9
So 1256355-53-9 is a valid CAS Registry Number.

1256355-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-(Benzyloxy)-3-fluorophenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 2-Benzyloxy-3-fluorophenylboronic 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:1256355-53-9 SDS

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