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2-(4-methoxyphenoxy)propanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

815622-52-7

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815622-52-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 815622-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,5,6,2 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 815622-52:
(8*8)+(7*1)+(6*5)+(5*6)+(4*2)+(3*2)+(2*5)+(1*2)=157
157 % 10 = 7
So 815622-52-7 is a valid CAS Registry Number.

815622-52-7SDS

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-(4-methoxyphenoxy)propanamide

1.2 Other means of identification

Product number -
Other names -

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:815622-52-7 SDS

815622-52-7Relevant academic research and scientific papers

Design, synthesis, and pharmacological effects of structurally simple ligands for MT1 and MT2 melatonin receptors

Carocci, Alessia,Catalano, Alessia,Lovece, Angelo,Lentini, Giovanni,Duranti, Andrea,Lucini, Valeria,Pannacci, Marilou,Scaglione, Francesco,Franchini, Carlo

, p. 6496 - 6511 (2010)

A series of phenoxyalkyl and phenylthioalkyl amides were prepared as melatoninergic ligands. Modulation of affinity of the newly synthesized compound by applying SARs around the terminal amide moiety, the alkyl chain, and the methoxy group on the aromatic ring provides compounds with nanomolar affinity for both melatonin receptor subtypes. Affinity towards MT1 and MT2 receptors were modulated also exploiting chirality. The investigation of intrinsic activity revealed that all the tested compounds behave as full or partial agonists.

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