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66502-26-9

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66502-26-9 Usage

Physical state

Yellow to brown solid

Uses

Building block for various pharmaceuticals and agrochemicals

Chemical structure

Contains a morpholine ring and a phenylethanone moiety

Synthesis applications

Useful intermediate for the synthesis of heterocyclic compounds and other organic molecules

Biological activities

Potential anti-inflammatory and anti-cancer properties

Importance in organic chemistry

Important reagent for the production of a wide range of compounds

Check Digit Verification of cas no

The CAS Registry Mumber 66502-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,0 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66502-26:
(7*6)+(6*6)+(5*5)+(4*0)+(3*2)+(2*2)+(1*6)=119
119 % 10 = 9
So 66502-26-9 is a valid CAS Registry Number.

66502-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-morpholin-4-yl-1-phenylethanone,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-morpholino-1-phenyl-2-thioxo-1-ethanone

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:66502-26-9 SDS

66502-26-9Upstream product

66502-26-9Relevant articles and documents

Hydantoin derivatives as potential antiinflammatory agents

Schulte,Von Weissenborn,Kwon

, p. 25 - 31 (2007/10/05)

The hydantoins 2a-c and three hydantoic acids were synthesized and their anti-inflammatory properties were determined in the rat paw oedema test. Neither 1-phenyl-sulphonyl-5,5-diphenylhydantoin, which has been described as an inflammatory, nor any of the other compounds, showed significant anti-inflammatory activity.

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