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2-{[3-(dimethylamino)phenyl]amino}benzoic acid is a complex organic compound with the molecular formula C15H16N2O3. It is characterized by a benzoic acid backbone, with an amino group attached to the 2-position. This amino group is further connected to a phenyl ring at the 3-position, which itself is substituted with a dimethylamino group. The compound is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of certain drugs. Its structure provides a foundation for understanding its chemical properties and reactivity, which can be crucial in drug development and other chemical applications.

3975-67-5

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3975-67-5 Usage

Derivative of benzoic acid

2-[3-(dimethylamino)phenyl]aminobenzoic acid is derived from benzoic acid, which is a simple aromatic carboxylic acid.

Contains a phenylamino group

The compound has a phenylamino group (-NH-C6H5) attached to it, which is an amino group connected to a phenyl ring.

Contains a dimethylamino group

It also has a dimethylamino group (-N(CH3)2) in its structure, which is an amino group with two methyl groups attached to it.

Commonly used in chemistry

2-[3-(dimethylamino)phenyl]aminobenzoic acid is frequently used in the field of chemistry, particularly in organic synthesis and pharmaceutical research.

Potential applications in drug development

The compound has the potential to be used in the development of new drugs due to its unique structure and properties.

Manufacturing of dyes and pigments

It can also be used in the production of dyes and pigments, which are important for various industries.

Valuable for scientific and industrial purposes

The unique structure and properties of 2-[3-(dimethylamino)phenyl]aminobenzoic acid make it a valuable compound for a wide range of scientific and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3975-67-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,7 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3975-67:
(6*3)+(5*9)+(4*7)+(3*5)+(2*6)+(1*7)=125
125 % 10 = 5
So 3975-67-5 is a valid CAS Registry Number.

3975-67-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-(dimethylamino)anilino]benzoic acid

1.2 Other means of identification

Product number -
Other names N-(3-Dimethylamino-phenyl)-anthranilsaeure

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:3975-67-5 SDS

3975-67-5Downstream Products

3975-67-5Relevant academic research and scientific papers

Structure-activity relationships in a series of anti-inflammatory N-arylanthranilic acids

Kaltenbronn,Scherrer,Short,Jones,Beatty,Saka,Winder,Wax,Williamson

, p. 621 - 627 (2007/10/02)

A large series of N-arylanthranilic acids has been prepared. Many of these compounds show high anti-inflammatory activity as measured by the anti-UV-erythema test. From this series have come the clinically useful nonsteroidal anti-inflammatory agents, flufenamic acid (Arlef), mefenamic acid (Ponstel), and the latest and most potent agent, N-(2,6-dichloro-m-tolyl)anthranilic acid (meclofenamic acid, Meclomen = the sodium salt). The structure-activity relationships of this series is discussed and a graphical representation is presented which allows the prediction of activity of new agents.

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