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2,5-dioxo-2,5-dihydrofuran-3,4-diyl diacetate is a chemical compound with the molecular formula C8H8O6. It is a derivative of furan, a heterocyclic organic compound consisting of a five-membered ring with four carbon atoms and one oxygen atom. In this specific compound, the furan ring is dihydroxylated, meaning it has two hydroxyl groups attached to it, and these hydroxyl groups are further esterified with acetic acid, resulting in the formation of two acetate groups. 2,5-dioxo-2,5-dihydrofuran-3,4-diyl diacetate is known for its potential applications in the synthesis of various organic compounds and pharmaceuticals, as well as its use as an intermediate in chemical reactions. Due to its complex structure and reactivity, it is typically handled by professionals in a controlled laboratory environment.

132-79-6

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132-79-6 Usage

Derived from furan

A heterocyclic organic compound consisting of a five-membered ring with one oxygen atom.

Cyclic ester

A type of ester that forms a cyclic structure.

Organic synthesis reagent

Commonly used in organic synthesis to produce various other organic compounds.

Building block

Can be employed as a starting material for the preparation of other organic compounds.

Pharmaceutical production

Used in the manufacturing of pharmaceuticals.

Fine chemicals intermediate

A useful intermediate in the production of fine chemicals.

Physical properties

A colorless liquid with a fruity odor.

Stability

Considered stable under normal conditions.

Handling and storage

Should be handled with care and stored in a cool, dry place away from heat and ignition sources.

Check Digit Verification of cas no

The CAS Registry Mumber 132-79-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132-79:
(5*1)+(4*3)+(3*2)+(2*7)+(1*9)=46
46 % 10 = 6
So 132-79-6 is a valid CAS Registry Number.

132-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-acetyloxy-2,5-dioxofuran-3-yl) acetate

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:132-79-6 SDS

132-79-6Downstream Products

132-79-6Relevant academic research and scientific papers

Hydrated Oxocarbons,IV. Silylation of 1,1-Dihydroxy Compounds.

Yalpani, Mohamed,Wilke, Guenther

, p. 661 - 669 (2007/10/02)

The action of various silylating agents on mono- and polyvicinal 1,1-dihydroxy compounds has been investigated.Some of these reagents converted ninhydrin (2) and rhodizonic acid (17) into the corresponding geminal bis(trimethylsilyloxy) derivatives 1 and 20, respectively.Compound 1 readily fragments to form hexamethyldisiloxan and indantrione (4).The rhodizonic acid derivative 20 is, however, rather stable and even on pyrolysis at 500 deg C gives only traces of the tetraketone 21.With other silylating agents unexpected C-alkylation or C-amidation at the dihydroxy carbon is observed.Silylation of perhydroxycyclobutane and -cyclohexane leads to ring opened and contracted products.

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