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182344-21-4

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182344-21-4 Usage

Uses

4-Hydroxy-3-methoxyphenylboronic acid is a useful reagent for organic synthesis and other chemical processes. It is used as a reagent in the synthesis of 4-arylcoumarins with antiprotozoal activity via Suzuki-Miyaura cross-coupling reaction, and in the direct palladium-catalyzed C-H functionalization of benzoquinones.

Check Digit Verification of cas no

The CAS Registry Mumber 182344-21-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,3,4 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 182344-21:
(8*1)+(7*8)+(6*2)+(5*3)+(4*4)+(3*4)+(2*2)+(1*1)=124
124 % 10 = 4
So 182344-21-4 is a valid CAS Registry Number.

182344-21-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Hydroxy-3-methoxyphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 3-methoxy-4-hydroxyphenyl 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:182344-21-4 SDS

182344-21-4Relevant articles and documents

Simple preparation of phenylpropenoid β-D-glucopyranoside congeners by Mizoroki-Heck type reaction using organoboron reagents

Kishida, Masashi,Akita, Hiroyuki

, p. 10559 - 10568 (2007/10/03)

Palladium(II)-catalyzed carbon-carbon bond formation between allyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside (3) and arylboronic acid congeners gave the corresponding cinnamyl 2,3,4,6-tetra-O-acetyl- β-d-glucopyranosides (4a-m) in good yield. Among them, coupling products 4a-m were converted to not only the naturally occurring phenylpropenoid β-d-glucopyranoside analogues (1a-e) but also the unnaturally ones (1f-m).

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