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(2,3-dimethoxy-5-methylphenyl)boronic acid(SALTDATA: FREE) is a boronic acid derivative with the molecular formula C9H13BO4. It features a phenyl ring with two methoxy and one methyl group attached, making it a versatile chemical compound for various applications in organic synthesis, pharmaceuticals, and material science.

396102-17-3

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396102-17-3 Usage

Uses

Used in Organic Synthesis:
(2,3-dimethoxy-5-methylphenyl)boronic acid(SALTDATA: FREE) is used as a reagent in the Suzuki-Miyaura cross-coupling reaction, a widely employed method for the formation of carbon-carbon bonds in organic chemistry. This reaction is crucial for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
(2,3-dimethoxy-5-methylphenyl)boronic acid(SALTDATA: FREE) serves as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, (2,3-dimethoxy-5-methylphenyl)boronic acid(SALTDATA: FREE) is utilized as a starting material for the development of new agrochemicals, such as pesticides and herbicides, to improve crop protection and yield.
Used in Antitumor Research:
(2,3-dimethoxy-5-methylphenyl)boronic acid(SALTDATA: FREE) has been studied for its potential antitumor activities, indicating its possible use in the development of new cancer treatments.
Used in Antiviral Research:
(2,3-dimethoxy-5-methylphenyl)boronic acid(SALTDATA: FREE) has also shown promise in antiviral research, suggesting its potential application in the development of new antiviral drugs to combat viral infections.
Used in Material Science for Electronic Devices:
Furthermore, (2,3-dimethoxy-5-methylphenyl)boronic acid(SALTDATA: FREE) has demonstrated potential in the development of new materials for electronic devices, contributing to advancements in technology and electronics manufacturing.

Check Digit Verification of cas no

The CAS Registry Mumber 396102-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,6,1,0 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 396102-17:
(8*3)+(7*9)+(6*6)+(5*1)+(4*0)+(3*2)+(2*1)+(1*7)=143
143 % 10 = 3
So 396102-17-3 is a valid CAS Registry Number.

396102-17-3SDS

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 (2,3-Dimethoxy-5-methylphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names -

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:396102-17-3 SDS

396102-17-3Upstream product

396102-17-3Relevant academic research and scientific papers

New route to herbertanes via a Suzuki cross-coupling reaction: Synthesis of herbertenediol

Abad, Antonio,Agulló, Consuelo,Cu?at, Ana C,Jiménez, Diego,Perni, Remedios H

, p. 9727 - 9735 (2007/10/03)

The synthesis of herbertenediol, a relevant member of the herbertane-type sesquiterpene family, is described. The synthesis is based on a new general approach to this group of sesquiterpenes where the herbertane skeleton is constructed using a Suzuki cross-coupling reaction and a [2,3]-sigmatropic Still-Wittig rearrangement as key synthetic steps.

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