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Ethyl 2-(dimethylamino)-3,6-diphenyl-2H-pyran-5-carboxylate is a complex organic compound with the molecular formula C21H21NO3. It is a derivative of pyran, a heterocyclic compound with a six-membered ring containing one oxygen atom. The structure of ethyl 2-(dimethylamino)-3,6-diphenyl-2H-pyran-5-carboxylate features a dimethylamino group (-N(CH3)2) at the 2-position, two phenyl groups (C6H5) at the 3 and 6 positions, and a carboxylate group (-COO-) at the 5-position. This molecule is an ester, formed by the reaction of the carboxylic acid group with ethanol (ethyl group -CH2CH3). Ethyl 2-(dimethylamino)-3,6-diphenyl-2H-pyran-5-carboxylate is a colorless solid and is used in various chemical and pharmaceutical applications, such as the synthesis of dyes, pigments, and pharmaceutical intermediates. Its unique structure and properties make it an important compound in the field of organic chemistry.

5195-16-4

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5195-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5195-16-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,9 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5195-16:
(6*5)+(5*1)+(4*9)+(3*5)+(2*1)+(1*6)=94
94 % 10 = 4
So 5195-16-4 is a valid CAS Registry Number.

5195-16-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(dimethylamino)-3,6-diphenyl-2H-pyran-5-carboxylate

1.2 Other means of identification

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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

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More Details:5195-16-4 SDS

5195-16-4Downstream Products

5195-16-4Relevant academic research and scientific papers

Reactivity of Arylic Carbanions Generated by Reductive Cleavage of C-N Bond of N,N-Dimethylanilines

Azzena, Ugo,Cattari, Manuela,Melloni, Giovanni,Pisano, Luisa

, p. 2811 - 2814 (2003)

Phenyl-substituted N,N-dimethylanilines, synthesized by Suzuki coupling reactions in good yields, are transformed to their corresponding arylic carbanions by reductive C-N cleavage with lithium at room temperature. These carbanions react with various elec

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