Welcome to LookChem.com Sign In|Join Free
  • or
5-Hydroxy-3-Methyl-2(5H)-furanone is a heterocyclic organic compound with a furan ring structure, featuring a hydroxyl group and a methyl group as substituents. It is known for its unique chemical properties and potential applications in various fields.

931-23-7

Post Buying Request

931-23-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

931-23-7 Usage

Uses

Used in Chemical Synthesis:
5-Hydroxy-3-Methyl-2(5H)-furanone is used as a reactant/reagent for synthetic preparation, specifically for the enantioselective preparation of hydroxy-GR24 stereoisomers via contra-biomimetic nucleophilic cyclization. This application is significant in the field of organic chemistry, where the synthesis of specific stereoisomers is crucial for the development of pharmaceuticals and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Hydroxy-3-Methyl-2(5H)-furanone is used as a key intermediate in the synthesis of various drug molecules. Its unique structure and reactivity make it a valuable building block for the development of new medications with improved efficacy and selectivity.
Used in Flavor and Fragrance Industry:
5-Hydroxy-3-Methyl-2(5H)-furanone is also used as a flavoring agent and a fragrance ingredient in the food and cosmetics industries. Its distinct aroma and taste profile contribute to the creation of unique and appealing sensory experiences in various products.
Used in Material Science:
In the field of material science, 5-Hydroxy-3-Methyl-2(5H)-furanone can be utilized as a component in the development of novel materials with specific properties, such as polymers with tailored characteristics for use in coatings, adhesives, or other industrial applications.
Overall, 5-Hydroxy-3-Methyl-2(5H)-furanone is a versatile compound with a wide range of applications across different industries, including chemical synthesis, pharmaceuticals, flavor and fragrance, and material science. Its unique structure and properties make it an important player in the development of innovative products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 931-23-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 931-23:
(5*9)+(4*3)+(3*1)+(2*2)+(1*3)=67
67 % 10 = 7
So 931-23-7 is a valid CAS Registry Number.

931-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-4-methyl-2H-furan-5-one

1.2 Other means of identification

Product number -
Other names 5-hydroxy-3-methyl-5H-furan-2-one

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:931-23-7 SDS

931-23-7Relevant academic research and scientific papers

Synthesis of a 13C-labelled seed-germination inhibitor (3,4,5-trimethylfuran-2(5H)-one) for the mode of action elucidation

Po?ta, Martin,Soós, Vilmos,Beier, Petr

, p. 1475 - 1480 (2018/04/16)

Abstract: It has been found that the butenolide 3,4,5-trimethylfuran-2(5H)-one, isolated from plant-derived smoke, efficiently inhibits seed germination and significantly reduces the effect of the highly active germination promotor karrikinolide (KAR

Compositions of retinoids substituted with a dithiane ring, their use, and process for preparing the compounds

-

, (2008/06/13)

The invention relates to a stereospecific derivative of formula: STR1 in which R is hydrogen or a C 1 -C 4 thioalkyl. The invention also relates to the use of these compounds for the manufacture of stereospecific retinal or retinoic acid, as well as to a process for preparing the retinoids of formula (I). The invention finally relates to a cosmetic or pharmaceutcial composition which contains at least one compound of formula (I) in a suitable vehicle; the pharmaceutical composition according to the invention may be used for treating dermatological, rheumatic, respiratory or ophthalmological conditions.

Propenals substituted with a dithiane ring and processes for the preparation of these propenals

-

, (2008/06/13)

Propenals of formula: STR1 in which formula R is H or a C1 -C4 thioalkyl radical, the dithiane ring being at the cis position in relation to the aldehyde function when R is H and at the trans position when R is a thioalkyl radical. The invention also relates to two processes for the preparation of these propenals.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 931-23-7