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3,4-dihydro-2H-pyran-4-yl acetate is an organic compound with the chemical formula C8H12O3. It is a derivative of pyran, a heterocyclic compound consisting of a six-membered ring with one oxygen atom. This specific compound features a 3,4-dihydro-2H-pyran-4-yl group attached to an acetate group, which is an ester formed from acetic acid and an alcohol. It is a colorless liquid with a fruity odor and is used as a synthetic flavoring agent in the food and beverage industry, as well as a fragrance component in the perfumery sector. The compound is also known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals.

5331-58-8

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5331-58-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5331-58-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5331-58:
(6*5)+(5*3)+(4*3)+(3*1)+(2*5)+(1*8)=78
78 % 10 = 8
So 5331-58-8 is a valid CAS Registry Number.

5331-58-8SDS

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 3,4-dihydro-2H-pyran-4-yl acetate

1.2 Other means of identification

Product number -
Other names 4-acetoxy-5,6-dihydro-4H-pyran

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:5331-58-8 SDS

5331-58-8Relevant academic research and scientific papers

PALLADIUM(0) ASSISTED SYNTHESIS OF C-GLYCOPYRANOSYL COMPOUNDS

Dunkerton, Lois V.,Euske, Jack M.,Serino, Anthony J.

, p. 89 - 108 (2007/10/02)

Tetrakis(triphenylphosphine)palladium(0) effects the regio- and stereo-selective alkylation of 2-acetoxy-5,6-dihydro-2H-pyrans and 1-S-acetyl-1-thiohex-2-enopyranosides.Use of stabilized carbanions resulted in the formation of alkylated dihydropyrans with

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