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5437-40-1

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5437-40-1 Usage

Chemical Structure

A benzene ring with a carboxylic acid group ( -\textCOOH ) at the 1-position,
An amino group ( -\textNH2 ) at the 2-position,
An ethyl group ( -\textC2\textH5 ) at the 3-position.

Derivative of

Benzoic acid

Applications

Production of pharmaceuticals
Production of dyes
Potential applications in organic synthesis

Physical Properties

Appearance: White to off-white crystalline solid
Odor: Slightly sweet
Solubility: Soluble in water and most organic solvents

Hazards

May pose hazards if ingested, inhaled, or comes into contact with skin or eyes

Safety Precautions

Proper safety precautions should be taken when handling this compound

Check Digit Verification of cas no

The CAS Registry Mumber 5437-40-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5437-40:
(6*5)+(5*4)+(4*3)+(3*7)+(2*4)+(1*0)=91
91 % 10 = 1
So 5437-40-1 is a valid CAS Registry Number.

5437-40-1SDS

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-3-ethylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3-ethyl-aniline

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:5437-40-1 SDS

5437-40-1Relevant articles and documents

Deamination of 1-alkyl-9-aminomethyltriptycenes. Participation of a neighboring 1-alkyl substituent

Yamamoto, Gaku,Koseki, Ai,Sugita, Jun,Mochida, Hisashi,Minoura, Mao

, p. 1585 - 1600 (2007/10/03)

Deamination reactions of 1-alkyl-9-aminomethyltriptycenes (alkyl = Me, Et, i-Pr, and t-Bu) and 9-(1-aminoethyl)-1-methyltriptycene were performed in CHCl3 and in AcOH, and product distributions were studied. The results suggest that the loss of

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