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Diethyl tetrahydro-2H-pyran-2-ylpropanedioate is a complex organic compound with the chemical formula C13H22O5. It is a colorless liquid with a molecular weight of 258.31 g/mol. diethyl tetrahydro-2H-pyran-2-ylpropanedioate is characterized by its ester functional group and a tetrahydro-2H-pyran ring, which contributes to its unique chemical properties. It is synthesized through the reaction of diethyl malonate with 3,4-dihydro-2H-pyran, and is used as an intermediate in the synthesis of various pharmaceuticals and other organic compounds. Due to its reactivity, it is typically handled under controlled conditions and is not found in nature.

5468-59-7

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5468-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5468-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5468-59:
(6*5)+(5*4)+(4*6)+(3*8)+(2*5)+(1*9)=117
117 % 10 = 7
So 5468-59-7 is a valid CAS Registry Number.

5468-59-7SDS

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 diethyl 2-(oxan-2-yl)propanedioate

1.2 Other means of identification

Product number -
Other names diethyl tetrahydro-2h-pyran-2-ylpropanedioate

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 -
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More Details:5468-59-7 SDS

5468-59-7Downstream Products

5468-59-7Relevant academic research and scientific papers

Addition of carbon nucleophiles to cyclic N-acyliminium and oxocarbenium ions under solvent-free conditions

de Godoy, Luiz Antonio F.,Camilo, Nilton Soares,Pilli, Ronaldo Aloise

, p. 7853 - 7856 (2007/10/03)

The InCl3-catalyzed addition of carbon nucleophiles to cyclic N-acyliminium and oxocarbenium ions under solvent-free conditions at room temperature is described. The corresponding α-substituted heterocycles were obtained in moderate to excellen

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