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Ethanimidamide, N'-(4-methoxyphenyl)-N,N-dimethyl-, also known as N,N-dimethyl-N'-(4-methoxyphenyl)ethanimidamide, is a chemical compound with the molecular formula C11H16N2O2. It is a derivative of ethanimidamide, featuring a 4-methoxyphenyl group attached to the nitrogen atom. Ethanimidamide, N'-(4-methoxyphenyl)-N,N-dimethyl- is characterized by its potential applications in pharmaceutical research, particularly in the development of drugs targeting various biological processes. Its structure, which includes a methoxy group on the phenyl ring, may influence its chemical properties and interactions with biological targets. The compound's specific role and effectiveness in such applications are subjects of ongoing scientific investigation.

4023-16-9

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4023-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4023-16-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4023-16:
(6*4)+(5*0)+(4*2)+(3*3)+(2*1)+(1*6)=49
49 % 10 = 9
So 4023-16-9 is a valid CAS Registry Number.

4023-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(4-methoxyphenyl)-N,N-dimethylethanimidamide

1.2 Other means of identification

Product number -
Other names N'-(4-methoxy-phenyl)-N,N-dimethyl-acetamidine

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:4023-16-9 SDS

4023-16-9Downstream Products

4023-16-9Relevant academic research and scientific papers

AMIDINES. PART 13. INFLUENCE OF SUBSTITUTION AT IMINO NITROGEN ATOM ON pKa VALUES OF N1N1-DIMETHYLACETAMIDINES

Oszczapowicz, Janusz,Raczynska, Ewa

, p. 1643 - 1646 (2007/10/02)

20 N1N1-Dimethylacetamidines containing alkyl, aralkyl, or substituted phenyl groups have been synthesized, and their pKa values in 95.6percent ethanol (azeotrope) measured.The pKa values obtained were correlated with Hammett ? constants.The applicability of various ? values is discussed, and it is shown that for substituents at nitrogen ?o values should be used.It has also been shown that the pKa values of amidines correlate well with the pKa values of corresponding primary amines, and that this correlation can serve for the prediction of the pKa of amidine.Comparison of the correlations for N1N1-dimethylacetamidines with those for N1N1-dimethylformamidines indicate that sensitivity of the amidine group to substitution at the imino nitrogen atom depends to a considerable degree on substitution at a functional carbon atom.

A REINVESTIGATION OF THE REACTION OF HMPA WITH KETOXIMES

Gupton, John T.,Idoux, John P.,Leonard, Russell,DeCrescenzo, Gary

, p. 1083 - 1094 (2007/10/02)

A series of ketoximes have been found to react with HMPA in the absence of acid catalysis to produce N,N-dimethyl-N'-arylamidines in reasonable yields.

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