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2,5-dihydro-2,5-dimethoxy-2,5-dimethylfuran is an organic compound characterized by the molecular formula C8H14O3. It is a derivative of furan, featuring both methoxy and methyl groups attached to its structure. 2,5-dihydro-2,5-dimethoxy-2,5-dimethylfuran is known for its sweet, aromatic odor, reminiscent of vanilla, which makes it a valuable ingredient in the flavoring of food products.

18091-25-3

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18091-25-3 Usage

Uses

Used in Food Industry:
2,5-dihydro-2,5-dimethoxy-2,5-dimethylfuran is used as a flavoring agent for imparting a vanilla-like flavor to various food products, particularly in the production of baked goods and confectionery. Its sweet and aromatic properties enhance the taste and aroma of these items, contributing to a more enjoyable consumer experience.
Used in Pharmaceutical and Medicinal Applications:
2,5-dihydro-2,5-dimethoxy-2,5-dimethylfuran is also being studied for its potential in the development of new drugs for various therapeutic uses. Its unique chemical structure and properties make it a promising candidate for pharmaceutical research, with the aim of discovering novel treatments for a range of medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 18091-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,9 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18091-25:
(7*1)+(6*8)+(5*0)+(4*9)+(3*1)+(2*2)+(1*5)=103
103 % 10 = 3
So 18091-25-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O3/c1-7(9-3)5-6-8(2,10-4)11-7/h5-6H,1-4H3

18091-25-3SDS

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 2,5-dimethoxy-2,5-dimethylfuran

1.2 Other means of identification

Product number -
Other names 2,5-dimethoxy-2,5-dimethyl-2,5-dihydro-furan

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:18091-25-3 SDS

18091-25-3Relevant academic research and scientific papers

Reaction of dialkylfurans with magnesium monoperoxyphthalate in MeOH: A new convenient approach to 2,5-dimethoxy-2,5-dihydrofurans

D'Annibale, Andrea,Scettri, Arrigo

, p. 4659 - 4660 (1995)

Dialkylfurans were reacted with magnesium monoperoxyphthlate (MMPP) in methanol to give 2,5-dimethoxy-2,5-dihydrofurans in high yields under mild reaction conditions.

The binary reagent PhI(OAc)2-Mg(ClO4)2: a SET induced ring enlargement of furan derivatives into pyranones

De Mico,Margarita,Piancatelli

, p. 3553 - 3556 (2007/10/02)

The binary reagent PhI(OAc)2-Mg(ClO4)2 is very efficient for a high conversion of (2-furyl)-1-alcohols into puranones. The reaction mechanism can be explained in terms of a SET process, with the generation of a cation radical as key intermediate.

A PHOTO-OXIDATIVE ANALOGUE OF THE CLAUSON-KAAS REACTION

Feringa, Ben L.,Butselaar, Robert J.

, p. 1941 - 1942 (2007/10/02)

2,5-Dimethoxy-2,5-dihydrofurans and spiroketals are obtained upon V2O5-catalysed degradation of hydroperoxides formed in furan photo-oxidations.

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