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4445-39-0

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4445-39-0 Usage

Structure

Derivative of benzoic acid with a phenyl group and an amino group attached to the benzene ring.

Applications

Synthesis of pharmaceuticals
Intermediate in the production of dyes and pigments

Therapeutic Potential

Studied for potential therapeutic effects in various medical applications.

Importance

Key in organic synthesis
Utilized in various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 4445-39-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4445-39:
(6*4)+(5*4)+(4*4)+(3*5)+(2*3)+(1*9)=90
90 % 10 = 0
So 4445-39-0 is a valid CAS Registry Number.

4445-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-3-phenylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3-phenylanthranilic 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:4445-39-0 SDS

4445-39-0Relevant articles and documents

Efficient synthesis of substituted biaryl anilines and biaryl phenols via a Suzuki cross-coupling reaction

Liu, Bin,Moffett, Kristofer K.,Joseph, Rhoda W.,Dorsey, Bruce D.

, p. 1779 - 1782 (2005)

An efficient synthesis of biaryl building blocks with multiple point diversities via a Suzuki cross-coupling reaction using a commercially available preformed Pd catalyst 1 was reported. Substituted biaryl anilines and phenols were obtained in one step from commercially available aryl halides.

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