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3-Acetoxy-4-methoxyphenylboronic acid, pinacol ester is an organic compound that belongs to the family of boronic acid pinacol esters. It is characterized by the presence of a boronic acid group and a pinacol ester group, which provide reactivity and stability, respectively. 3-ACETOXY-4-METHOXYPHENYLBORONIC ACID, PINACOL ESTER is widely used as a versatile building block in organic synthesis, particularly in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its unique structure and properties make it a valuable tool for the preparation of important organic molecules.

917757-44-9

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917757-44-9 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Acetoxy-4-methoxyphenylboronic acid, pinacol ester is used as a key reagent in the synthesis of pharmaceuticals for its ability to form carbon-carbon bonds through Suzuki-Miyaura coupling reactions. This allows for the creation of complex organic molecules with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 3-Acetoxy-4-methoxyphenylboronic acid, pinacol ester is used as a building block for the development of new agrochemicals. Its reactivity in Suzuki-Miyaura coupling reactions enables the synthesis of novel compounds with potential applications in crop protection and pest control.
Used in Materials Science:
3-Acetoxy-4-methoxyphenylboronic acid, pinacol ester is utilized in materials science as a component in the synthesis of advanced materials. Its unique structure and reactivity contribute to the development of materials with specific properties, such as conductivity, stability, or biocompatibility, for various applications in fields like electronics, energy, and medicine.
Used in Organic Synthesis:
As a member of the boronic acid pinacol esters family, 3-Acetoxy-4-methoxyphenylboronic acid, pinacol ester is used as a versatile building block in organic synthesis. Its reactivity in Suzuki-Miyaura coupling reactions allows for the formation of carbon-carbon bonds, facilitating the synthesis of a wide range of organic molecules with diverse applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 917757-44-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,7,5 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 917757-44:
(8*9)+(7*1)+(6*7)+(5*7)+(4*5)+(3*7)+(2*4)+(1*4)=209
209 % 10 = 9
So 917757-44-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H21BO5/c1-10(17)19-13-9-11(7-8-12(13)18-6)16-20-14(2,3)15(4,5)21-16/h7-9H,1-6H3

917757-44-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names 3-Acetoxy-4-methoxyphenylboronic acid pinacol ester

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:917757-44-9 SDS

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