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404009-46-7

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404009-46-7 Usage

Class

Ketones

Structure

Contains a phenyl ring with a morpholine and a hydroxy group attached

Usage

Pharmaceutical intermediate in the synthesis of various drugs and pharmaceutical compounds

Application

Development of new medications and treatments for various medical conditions

Utilization

Research and development laboratories for scientific studies

Health hazards

Potential health hazards due to its complex structure

Precautions

Use in well-ventilated areas, wear appropriate personal protective equipment (PPE), and follow proper disposal procedures

Check Digit Verification of cas no

The CAS Registry Mumber 404009-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,0,0 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 404009-46:
(8*4)+(7*0)+(6*4)+(5*0)+(4*0)+(3*9)+(2*4)+(1*6)=97
97 % 10 = 7
So 404009-46-7 is a valid CAS Registry Number.

404009-46-7SDS

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-hydroxy-4-morpholin-4-ylphenyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names AMA37

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:404009-46-7 SDS

404009-46-7Downstream Products

404009-46-7Relevant articles and documents

One-pot, modular approach to functionalized ketones via nucleophilic addition/Buchwald-Hartwig amination strategy

De Jong, Jorn,Heijnen, Dorus,Helbert, Hugo,Feringa, Ben L.

, p. 2908 - 2911 (2019/03/17)

A general one-pot procedure for the 1,2-addition of organolithium reagents to amides followed by the Buchwald-Hartwig amination with in situ released lithium amides is presented. In this work amides are used as masked ketones, revealed by the addition of organolithium reagents which generates a lithium amide, suitable for subsequent Buchwald-Hartwig coupling in the presence of a palladium catalyst. This methodology allows for rapid, efficient and atom economic synthesis of aminoarylketones in good yields.

MATERIALS AND METHODS TO POTENTIATE CANCER TREATMENT

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, (2008/06/13)

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