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4-{4-[(2-chloroethyl)(ethyl)amino]phenyl}butanoic acid is a complex organic compound with the molecular formula C16H22ClNO2. It is a derivative of phenylbutanoic acid, featuring a chloroethyl and ethyl amino group attached to the phenyl ring. This chemical structure is significant in the field of pharmaceuticals, as it is a key component in the synthesis of certain drugs. The compound's properties, such as its reactivity and potential applications, are shaped by the presence of the chlorine atom and the amino group, which can participate in various chemical reactions. Its specific role and importance in the pharmaceutical industry are related to its ability to form stable bonds and its potential therapeutic effects, although further details on its specific applications or mechanisms of action would require more context or a specific reference to a particular drug or study.

6296-43-1

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6296-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6296-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6296-43:
(6*6)+(5*2)+(4*9)+(3*6)+(2*4)+(1*3)=111
111 % 10 = 1
So 6296-43-1 is a valid CAS Registry Number.

6296-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Phenyl-4-p-<N,N-bis-(2-chlor-ethyl)-amino>-benzyliden-oxazolon-(5)

1.2 Other means of identification

Product number -
Other names 4-{4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-2-phenyl-4H-oxazol-5-one

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:6296-43-1 SDS

6296-43-1Relevant academic research and scientific papers

Synthesis and evaluation of DNA-targeted spatially separated bis(aniline mustards) as potential alkylating agents with enhanced DNA cross-linking capability

Gourdie,Prakash,Wakelin,Woodgate,Denny

, p. 240 - 248 (2007/10/02)

DNA-targeted separated bis-mustards were synthesized by attaching aniline mono-mustards at the 4- and 9-positions of the DNA-intercalating ligand 9-aminoacridine-4-carboxamide, with the intention of improving the low cross-link to monoadduct ratio found w

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