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N-(2-Aminoethyl)-2-(2,6-dichlorophenoxy)propanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

344443-16-9

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344443-16-9 Usage

Chemical Properties

Dark-Red Oil

Uses

Lofexidine intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 344443-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,4,4 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 344443-16:
(8*3)+(7*4)+(6*4)+(5*4)+(4*4)+(3*3)+(2*1)+(1*6)=129
129 % 10 = 9
So 344443-16-9 is a valid CAS Registry Number.

344443-16-9SDS

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 N-(2-Aminoethyl)-2-(2,6-dichlorophenoxy)propanamide

1.2 Other means of identification

Product number -
Other names PRO035

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:344443-16-9 SDS

344443-16-9Downstream Products

344443-16-9Relevant academic research and scientific papers

PROCESS FOR THE SYNTHESIS OF LOFEXIDINE

-

Page/Page column 15, (2021/10/22)

The present invention relates to an improved process for the synthesis of lofexidine, or a pharmaceutically acceptable salt thereof, using an aluminium alkoxide as Lewis acid.

A scalable, enantioselective synthesis of the r2-adrenergic agonist, lofexidine

Vartak, Ashish P.,Crooks, Peter A.

body text, p. 415 - 419 (2010/04/22)

A scalable and high-yielding synthetic route toward pure enantiomers of the α2-adrenergic agonist, lofexidine hydrochloride, is presented. Salient features include a rapid one-pot amide alkylation-imidazoline formation sequence on the carboxami

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