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85107-51-3

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85107-51-3 Usage

Derivative of Benzoic Acid

Contains an amino group and a boron atom bonded to two hydroxyl groups

Potential Applications

Pharmaceuticals: Building block for drug development
Material Science: Potential applications in material science
Chemical Synthesis: Useful in chemical synthesis processes

Boron Atom Properties

Catalysis: Potential use in catalytic reactions
Lewis Acid: Acts as a Lewis acid in various chemical reactions

Versatile Properties

Valuable component for the development of new compounds in industrial and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 85107-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,0 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85107-51:
(7*8)+(6*5)+(5*1)+(4*0)+(3*7)+(2*5)+(1*1)=123
123 % 10 = 3
So 85107-51-3 is a valid CAS Registry Number.

85107-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4-boronobenzoic acid

1.2 Other means of identification

Product number -
Other names 4-BORONOANTHRANILIC 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:85107-51-3 SDS

85107-51-3Relevant articles and documents

Structural study of phenyl boronic acid derivatives as AmpC β-lactamase inhibitors

Tondi, Donatella,Calò, Samuele,Shoichet, Brian K.,Costi, Maria Paola

supporting information; experimental part, p. 3416 - 3419 (2010/08/19)

A small set of boronic acids acting as low nanomolar inhibitors of AmpC β-lactamase were designed and synthesized in the effort to improve affinity, pharmacokinetic properties, and to provide a valid lead compound. X-ray crystallography revealed the binar

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