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6-(ethoxycarbonyl)-4-oxo-4H-pyran-2-carboxylic acid is a complex organic compound with the molecular formula C9H8O6. It is a derivative of pyran-2-carboxylic acid, featuring a 4-oxo-4H-pyran-2-carboxylic acid core structure. The compound is characterized by the presence of an ethoxycarbonyl group (-COOCH2CH3) at the 6-position and a carbonyl group at the 4-position. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain antibiotics and other bioactive compounds. Its chemical properties and reactivity make it a valuable building block in organic synthesis, allowing for the creation of a wide range of molecules with diverse functionalities.

717-72-6

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717-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 717-72-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 717-72:
(5*7)+(4*1)+(3*7)+(2*7)+(1*2)=76
76 % 10 = 6
So 717-72-6 is a valid CAS Registry Number.

717-72-6SDS

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 6-(Ethoxycarbonyl)-4-oxo-4H-pyran-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Oxo-4H-pyran-2,6-dicarbonsaeure-monoaethylester

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

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More Details:717-72-6 SDS

717-72-6Relevant academic research and scientific papers

Synthesis of an 4-oxo-1,4-dihydropyridinomethylidene substituted 2-indolinone

Lumetzberger, Astrid,Loewe, Werner,Weber, Manuela,Luger, Peter

, p. 155 - 159 (2008/03/27)

(Chemical Equation Presented) The (Z)-3-substituted 2-indolinone 6 was prepared using the aldehydes 4 and 8 unknown up to now and 2-indolinone.

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