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68162-47-0

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68162-47-0 Usage

Chemical Properties

White solid

Uses

Different sources of media describe the Uses of 68162-47-0 differently. You can refer to the following data:
1. Reactant involved in:Design of boronic acid-based autotaxin inhibitorsSynthesis of boronated phosphonium saltsStudies of incorporation of boronic acid groups to enhance gene transfection capabilityInvestigations of the effect of boronic acid-positioning in optical glucose-sensing ensemble
2. Reactant involved in:? ;Design of boronic acid-based autotaxin inhibitors1? ;Synthesis of boronated phosphonium salts2? ;Studies of incorporation of boronic acid groups to enhance gene transfection capability2? ;Investigations of the effect of boronic acid-positioning in optical glucose-sensing ensemble3
3. suzuki reaction

General Description

May contain varying amounts of anhydride

Check Digit Verification of cas no

The CAS Registry Mumber 68162-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,6 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68162-47:
(7*6)+(6*8)+(5*1)+(4*6)+(3*2)+(2*4)+(1*7)=140
140 % 10 = 0
So 68162-47-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BBrO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4,10-11H,5H2

68162-47-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L19953)  4-(Bromomethyl)benzeneboronic acid, tech. 85%   

  • 68162-47-0

  • 1g

  • 1073.0CNY

  • Detail
  • Alfa Aesar

  • (L19953)  4-(Bromomethyl)benzeneboronic acid, tech. 85%   

  • 68162-47-0

  • 5g

  • 4338.0CNY

  • Detail

68162-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Bromomethyl)phenylboronic acid

1.2 Other means of identification

Product number -
Other names [4-(bromomethyl)phenyl]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:68162-47-0 SDS

68162-47-0Relevant articles and documents

Indole and quinoline derivatives and its preparation method and application

-

Paragraph 0243; 0246; 0247, (2017/02/28)

The invention provides an indoloquinoline derivative, a preparation method and application thereof in preparing antitumor drugs and antiviral drugs. The chemical structure of the indoloquinoline derivative is shown as a formula I. Experiments show that a partly-boric-acid-modified indoloquinoline derivative and a non-boric-acid-modified indoloquinoline derivative have strong inhibition effect on various tumor cell strains, thereby being capable of being used for preparation of the antitumor drugs, and have strong antiviral activity, thereby being capable of being used for preparation of the antiviral drugs.

Synthesis of (azidomethyl)phenylboronic acids

Fedorov,Shchepalov,Bol'shakov,Shavyrin,Kurskii,Finet,Zelentsov

, p. 370 - 375 (2007/10/03)

The synthesis of 2-, 3-, and 4-(azidomethyl)phenylboronic acids was carried out. The geometric and electronic structures were studied by quantum-chemical methods. The suggestion is made that there are weak intramolecular interactions between the boron atom and the nitrene nitrogen atom of the azido group.

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