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2-(5-[1,3]DIOXOLAN-2-YL-2,4-DIMETHOXY-PHENYL)-BORONIC ACID PINACOL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

552845-85-9

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  • 2-(5-[1,3]DIOXOLAN-2-YL-2,4-DIMETHOXY-PHENYL)-BORONIC ACID PINACOL ESTER

    Cas No: 552845-85-9

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552845-85-9 Usage

Boronic acid compound

Contains a boronic acid moiety, which is a versatile building block in organic synthesis.

Pinacol ester functional group

Often used as a protecting group in organic chemistry, allowing selective manipulation of other functional groups within a molecule.

Dimethoxyphenyl group

Aromatic compound containing two methoxy groups, which can be involved in various chemical reactions.

Dioxinane ring

A five-membered cyclic ether that can be used as a scaffold in the construction of complex molecules.

Potential applications

May have potential applications in medicinal chemistry, materials science, and other areas of chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 552845-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,2,8,4 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 552845-85:
(8*5)+(7*5)+(6*2)+(5*8)+(4*4)+(3*5)+(2*8)+(1*5)=179
179 % 10 = 9
So 552845-85-9 is a valid CAS Registry Number.

552845-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-[1,3]dioxolan-2-yl-2,4-dimethoxy-phenyl)-4,4,5,5-tetra-methyl-[1,3,2]dioxaborolane

1.2 Other means of identification

Product number -
Other names 2-(5-[1,3DIOXOLAN-2-YL-2,4-DIMETHOXY-PHENYL)-BORONIC 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:552845-85-9 SDS

552845-85-9Relevant articles and documents

Carboxylated, heteroaryl-substituted chalcones as inhibitors of vascular cell adhesion molecule-1 expression for use in chronic inflammatory diseases

Meng, Charles Q.,Ni, Liming,Worsencroft, Kimberly J.,Ye, Zhihong,Weingarten, M. David,Simpson, Jacob E.,Skudlarek, Jason W.,Marino, Elaine M.,Suen, Ki-Ling,Kunsch, Charles,Souder, Amy,Howard, Randy B.,Sundell, Cynthia L.,Wasserman, Martin A.,Sikorski, James A.

, p. 1304 - 1315 (2008/02/02)

Starting from a simple chalcone template, structure-activity relationship (SAR) studies led to a series of carboxylated, heteroaryl-substituted chalcone derivatives as novel, potent inhibitors of vascular cell adhesion molecule-1 (VCAM-1) expression. Corr

PROCESS OF MAKING CHALCOME DERIVATIVES

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Page 73-74, (2010/02/07)

This invention is a novel methods of manufacturing chalcones that includes reacting a carbon-linked heteroaryl or heterocyclic substituted benzaldehyde with an acetophenone in a solvent or mixture of solvents in the presence of LiOMe. Also provided are new chalcones for the treatment of medical conditions.

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