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15793-48-3

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15793-48-3 Usage

General Description

5-Chloro-2-ethoxyaniline, also known as 2-amino-5-chloroethylphenol, is an organic compound with the chemical formula C8H10ClNO. It is a derivative of aniline and features a chlorine atom at the fifth position and an ethoxy group at the second position of the phenyl ring. This chemical is commonly used in the synthesis of various pharmaceutical compounds and dyes. It is also used in the production of agrochemicals, rubber chemicals, and other organic chemicals. 5-Chloro-2-ethoxyaniline is a white to off-white crystalline solid with a slightly aromatic odor, and it should be handled and stored with proper caution due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 15793-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,9 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15793-48:
(7*1)+(6*5)+(5*7)+(4*9)+(3*3)+(2*4)+(1*8)=133
133 % 10 = 3
So 15793-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10ClNO/c1-2-11-8-4-3-6(9)5-7(8)10/h3-5H,2,10H2,1H3

15793-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-2-ethoxyaniline

1.2 Other means of identification

Product number -
Other names o-Phenethidine,5-chloro

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:15793-48-3 SDS

15793-48-3Relevant articles and documents

N4-Phenyl modifications of N2-(2-hydroxyl)ethyl-6-(pyrrolidin-1-yl)-1,3,5-triazine-2,4-d iamines enhance glucocerebrosidase inhibition by small molecules with potential as chemical chaperones for Gaucher disease

Huang, Wenwei,Zheng, Wei,Urban, Daniel J.,Inglese, James,Sidransky, Ellen,Austin, Christopher P.,Thomas, Craig J.

, p. 5783 - 5789 (2008/02/13)

A series of 1,3,5-triazine-2,4,6-triamines were prepared and analyzed as inhibitors of glucocerebrosidase. Synthesis, structure activity relationships and the selectivity of chosen analogues against related sugar hydrolases enzymes are described.

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