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214209-93-5

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214209-93-5 Usage

Type of compound

Ketone derivative

Contains

Bromine atom, morpholine ring

Usage

Building block in organic synthesis and medicinal chemistry

Potential

Interaction with biological targets, pharmacological activity

Useful for

Radiolabeling, chemical biology, drug discovery

Versatility

Potential applications in various fields of research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 214209-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,2,0 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 214209-93:
(8*2)+(7*1)+(6*4)+(5*2)+(4*0)+(3*9)+(2*9)+(1*3)=105
105 % 10 = 5
So 214209-93-5 is a valid CAS Registry Number.

214209-93-5SDS

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 2-(3-bromophenyl)-1-morholin-4-ylethanone

1.2 Other means of identification

Product number -
Other names 3-bromophenyl-1-morpholin-4-yl-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:214209-93-5 SDS

214209-93-5Relevant articles and documents

Substituted 4-anilino-7-phenyl-3-quinolinecarbonitriles as Src kinase inhibitors

Berger, Dan,Dutia, Minu,Powell, Dennis,Wissner, Allan,DeMorin, Frenel,Raifeld, Yuri,Weber, Jennifer,Boschelli, Frank

, p. 2989 - 2992 (2007/10/03)

A series of substituted 4-anilino-7-phenyl-3-quinolinecarbonitriles has been prepared as Src kinase inhibitors. Optimal activity is observed with compounds that have basic amines attached via the para position of the 7-phenyl ring, and a hydrogen atom at the C-6 position. The best compounds are low nanomolar inhibitors of Src kinase, and have potent activity against Src-transformed fibroblast cells.

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