65223-07-6

Basic information

• Product Name: 2-(1-hydroxy-3-butenyl)-5-methyl furan
• Synonyms: 2-(1-hydroxy-3-butenyl)-5-methyl furan
• CAS NO: 65223-07-6
• Molecular Formula: C9H12 O2
• Molecular Weight: 152.19
• Mol File: 65223-07-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(1-hydroxy-3-butenyl)-5-methyl furan(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1-hydroxy-3-butenyl)-5-methyl furan(65223-07-6)
• EPA Substance Registry System: 2-(1-hydroxy-3-butenyl)-5-methyl furan(65223-07-6)

Safety Data

• Hazardous Substances Data: 65223-07-6(Hazardous Substances Data)

Usage

Organic compound

It is an organic compound This means that it is primarily composed of carbon atoms along with hydrogen, oxygen, and other elements.

Furan ring

The compound contains a furan ring Furan is a heterocyclic aromatic compound with a five-membered ring containing one oxygen atom, which gives the compound its unique properties.

Hydroxybutenyl group

It has a hydroxybutenyl group attached A hydroxybutenyl group is a butenyl group (a four-carbon chain with one double bond) with a hydroxyl (-OH) group, contributing to its aromatic and flavor properties.

Methyl group

The compound also has a methyl group attached A methyl group (-CH3) is a carbon atom with three hydrogen atoms, adding to the compound's structure and properties.

Naturally occurring

It is commonly found in nature 2-(1-hydroxy-3-butenyl)-5-methyl furan is a component of various plant extracts, indicating that it is a naturally occurring compound.

Flavoring agent

Identified as a flavoring agent in certain foods The compound is used in the food and beverage industry to enhance the flavor of products like coffee and bread due to its aromatic properties.

Aromatic properties

The unique chemical structure and aromatic properties The combination of the furan ring, hydroxybutenyl group, and methyl group contribute to the compound's aromatic properties, making it useful as a flavor enhancer.

Potential applications in pharmaceutical and cosmetic industries

Due to its bioactive properties and pleasant aroma The compound's unique structure and properties make it a potential candidate for use in pharmaceutical and cosmetic products.

Upstream product

• 620-02-0 5-Methylfurfural 
• 4965-17-7 tetrapentylammonium chloride 
• 107-05-1 3-chloroprop-1-ene 
• 7440-66-6 zinc 
• 591-87-7 Allyl acetate 
• 1730-25-2 allylmagnesium bromide 
• 106-95-6 allyl bromide 
• 24850-33-7 allyltributylstanane 
• 2622-05-1 allylmagnesium bromide 

Downstream Products

• 77806-60-1 l-2-allyl-3-hydroxy-3-methyl-4-cyclopentenone 

Relevant articles and documents

Photocatalytic Umpolung Synthesis of Nucleophilic π-Allylcobalt Complexes for Allylation of Aldehydes

The concept of "umpolung"reactivity of π-allylmetal complexes has been developed as a powerful method for the allylation of aldehydes. This paper describes the photocatalytic umpolung strategy for the synthesis of nucleophilic allylcobalt complexes through a single-electron-transfer (SET) process. This strategy enables the metallaphotoredox allylation of carbonyls with allyl acetate using organic N,N-diisopropylethylamine as the terminal reductant bypassing the use of a stoichiometric amount of metals. Ultraviolet-visible spectroscopy was used to monitor the redox changes of cobalt in the reaction.

A catalytic enantioselective allylation reaction of aldehydes in an aqueous medium

A modified Yamamoto-Yanagisawa's catalyst (S)-Tol-BINAP·AgNO3 was successfully applied to a catalytic enantioselective allylation reaction of aldehydes in an aqueous system. The reactions with aromatic aldehydes afforded the desired products in

Method for producing furfuryl alcohols

A method for producing a furfuryl alcohol useful as an intermediate for producing agricultural chemicals, medicines, perfumes, etc., represented by the general formula (I), STR1 wherein R1 represents a hydrogen atom or a methyl group, and R2 represents an allyl or propargyl group, which comprises reacting a furfural represented by the general formula (II), STR2 wherein R1 has the same meaning as described above, with a halogen compound represented by the general formula, wherein X represents a halogen atom and R2 has the same meaning as described above, in water or a water/organic solvent mixed solvent in the presence of at least one organic quaternary ammonium salt selected from the group consisting of tetra(C2 -C5 alkyl)amonium halide, benzyltri (C2 -C3 alkyl)ammonium chloride, dodecyltrimethylammonium bromide and cetyltrimethylammonium chloride as well as an inorganic ammonium salt and zinc.