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4-Butoxy-3-fluorophenylboronic acid is a boronic acid derivative with the molecular formula C10H13BO3F. It features a butoxy group and a fluorophenyl group, and is widely utilized in organic synthesis for the preparation of pharmaceuticals, agrochemicals, and organic materials. Its capacity to form stable complexes with various organic substrates renders it a valuable reagent in cross-coupling and Suzuki-Miyaura coupling reactions. Additionally, it holds potential in the development of novel materials and as a tool for studying boron chemistry.

156487-13-7

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156487-13-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Butoxy-3-fluorophenylboronic acid is used as a building block for the synthesis of various pharmaceuticals, due to its ability to form stable complexes with organic substrates, facilitating the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Butoxy-3-fluorophenylboronic acid is employed as a key intermediate in the synthesis of agrochemicals, contributing to the creation of effective and environmentally friendly pesticides and herbicides.
Used in Organic Synthesis:
4-Butoxy-3-fluorophenylboronic acid is used as a reagent in cross-coupling reactions and Suzuki-Miyaura coupling reactions, enabling the formation of stable complexes with a variety of organic substrates and promoting the synthesis of complex organic molecules.
Used in Material Science:
In the field of material science, 4-Butoxy-3-fluorophenylboronic acid is utilized in the development of novel materials, leveraging its unique chemical properties to create innovative materials with enhanced performance characteristics.
Used in Boron Chemistry Research:
4-Butoxy-3-fluorophenylboronic acid serves as a potential tool in the study of boron chemistry, providing insights into the behavior and applications of boron-containing compounds in various chemical processes and reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 156487-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,4,8 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156487-13:
(8*1)+(7*5)+(6*6)+(5*4)+(4*8)+(3*7)+(2*1)+(1*3)=157
157 % 10 = 7
So 156487-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H14BFO3/c1-2-3-6-15-10-5-4-8(11(13)14)7-9(10)12/h4-5,7,13-14H,2-3,6H2,1H3

156487-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Butoxy-3-fluorophenyl)boronic acid

1.2 Other means of identification

Product number -
Other names (4-butoxy-3-fluorophenyl)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:156487-13-7 SDS

156487-13-7Downstream Products

156487-13-7Relevant academic research and scientific papers

LIQUID CRYSTALLINE COMPOUND HAVING NEGATIVE DIELECTRIC ANISOTROPY, AND LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT EACH COMPRISING SAME

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, (2012/01/11)

The invention provides a liquid crystal compound having general physical properties necessary for a liquid crystal compound, that is to say, stability to heat, light or the like, a small viscosity, a suitable value of refractive index anisotropy, a suitable value of dielectric anisotropy, steep characteristics electro-optic characteristics, a wide temperature range of a nematic phase and an excellent compatibility with other liquid crystal compounds, and a liquid crystal compounds especially having a wide temperature range of a nematic phase. A compound represented by formula (1). For example, R1 and R2 are each independently alkyl having 1 to 9 carbons or alkenyl having 2 to 9 carbons, alkoxy having 1 to 8 carbons or alkenyloxy having 2 to 8 carbons; Q1 and Q4 are each independently fluorine or chlorine; Q2 and Q3 are each independently hydrogen, fluorine or chlorine, and one of Q2 and Q3 is hydrogen; Z is -CH2O or -COO-; and h is 1 or 2.

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