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N,3-bis(4-methoxyphenyl)-N-[(4-methylphenyl)sulfonyl]prop-2-enamide is a complex organic compound with the molecular formula C23H23NO5S. It is characterized by the presence of two 4-methoxyphenyl groups attached to the nitrogen atom, a sulfonyl group connected to a 4-methylphenyl group, and a prop-2-enamide functional group. N,3-bis(4-methoxyphenyl)-N-[(4-methylphenyl)sulfonyl]prop-2-enamide is known for its potential applications in pharmaceuticals and chemical research, particularly in the development of new drugs and the study of molecular interactions. Its structure provides a unique set of properties that can be exploited in various chemical reactions and biological assays.

6873-56-9

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6873-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6873-56-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,7 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6873-56:
(6*6)+(5*8)+(4*7)+(3*3)+(2*5)+(1*6)=129
129 % 10 = 9
So 6873-56-9 is a valid CAS Registry Number.

6873-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,3-bis(4-methoxyphenyl)-N-(4-methylphenyl)sulfonylprop-2-enamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6873-56-9 SDS

6873-56-9Relevant academic research and scientific papers

Endocyclic Nucleophilic Substitution at Tetracoordinate Sulfur(VI)

Andersen, Kenneth K.,Chumpradit, Sumalee,McIntyre, Debra J.

, p. 4667 - 4675 (2007/10/02)

A search for endocyclic nucleophilic substitution at tetracoordinate sulfur(VI), usually sulfonyl sulfur, was carried out through the use of molecules so constructed that any intramolecular substitution process was forced to proceed through four-, five-,

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