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1296671-86-7

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1296671-86-7 Usage

Description

3-Pentyloxyphenylboronic acid is a boronic acid derivative with the molecular formula C12H17BO4. It is a white to off-white powder that is insoluble in water but soluble in organic solvents such as methanol and ethanol. This chemical compound is commonly used in organic synthesis as a reagent for the Suzuki coupling reaction, which involves the cross-coupling of aryl halides with arylboronic acids. Additionally, it serves as a ligand for transition metal-catalyzed cross-coupling reactions and as a precursor for the synthesis of various biologically active compounds. 3-Pentyloxyphenylboronic acid is considered stable under normal conditions of use and storage but may decompose when exposed to high temperatures or strong acids.

Uses

Used in Organic Synthesis:
3-Pentyloxyphenylboronic acid is used as a reagent in the Suzuki coupling reaction for the cross-coupling of aryl halides with arylboronic acids. This reaction is crucial in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials.
Used in Transition Metal-Catalyzed Cross-Coupling Reactions:
3-Pentyloxyphenylboronic acid is used as a ligand in transition metal-catalyzed cross-coupling reactions. These reactions are essential for the formation of carbon-carbon bonds in organic synthesis, allowing for the creation of complex molecular structures with potential applications in various industries.
Used in the Synthesis of Biologically Active Compounds:
3-Pentyloxyphenylboronic acid is used as a precursor for the synthesis of various biologically active compounds. These compounds may have potential applications in the pharmaceutical industry, such as the development of new drugs with therapeutic properties.
Used in the Chemical Industry:
3-Pentyloxyphenylboronic acid is used in the chemical industry for the production of various chemical intermediates and specialty chemicals. Its versatility as a reagent and ligand in cross-coupling reactions makes it valuable for the synthesis of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 1296671-86-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,6,6,7 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1296671-86:
(9*1)+(8*2)+(7*9)+(6*6)+(5*6)+(4*7)+(3*1)+(2*8)+(1*6)=207
207 % 10 = 7
So 1296671-86-7 is a valid CAS Registry Number.

1296671-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-pentoxyphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 3-Pentyloxyphenylboronic 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:1296671-86-7 SDS

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