106584-14-9

Basic information

• Product Name: 2-(2-FURYL)PHENOL
• Synonyms: AKOS BAR-1757;2-(2-FURYL)PHENOL;2-(furan-2-yl)phenol
• CAS NO: 106584-14-9
• Molecular Formula: C₁₀H₈O₂
• Molecular Weight: 160.17
• Mol File: 106584-14-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-FURYL)PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-FURYL)PHENOL(106584-14-9)
• EPA Substance Registry System: 2-(2-FURYL)PHENOL(106584-14-9)

Safety Data

• Hazardous Substances Data: 106584-14-9(Hazardous Substances Data)

Usage

Physical form

White crystalline solid, which describes the appearance and texture of the compound.

Usage in the food industry

As a flavor and fragrance ingredient, which indicates that it is used to add taste and smell to food products.

Aroma

Sweet, floral, which describes the scent of the compound.

Usage in perfumes and cosmetics

In the production of these products, which indicates that it is used as a fragrance ingredient.

Synthesis of other organic compounds

As a building block, which means that it is used as a starting material to create other chemical compounds.

Antimicrobial properties

The ability to kill or inhibit the growth of microorganisms, which makes it useful in some pharmaceutical and personal care products.

Potential health risks

Prolonged exposure may cause skin irritation and allergic reactions in some individuals, which indicates that it can be harmful to some people.

Upstream product

• 13331-23-2 fur-2-ylboronic acid 
• 533-58-4 2-Iodophenol 
• 106584-08-1 1-Methyl-2-(2-furylmethyl)pyridinium iodide 
• 135449-12-6 2-(2-Furyl)phenyl acetate 
• 5720-06-9 2-Methoxyphenylboronic acid 
• 38527-59-2 2-(2-methoxyphenyl)furan 

Downstream Products

• 1169976-90-2 (E)-1,2-dichloroethenyl 2-(2-furyl)phenyl ether 

Relevant articles and documents

Synthesis of complex fused polycyclic heterocycles utilizing IMDAF reactions of allylamino- or allyloxy-furyl(hetero)arenes

Arenes and heteroarenes carrying a halogen and an amino- or hydroxy group have been converted to allylamino- or allyloxy-furyl-(hetero)arenes. These compounds underwent IMDAF reactions to give complex fused polycyclic heterocycles. The reactivity of the s

The synthesis of 3-hydroxymethylfuro[3,2-b]naphtho[2,3-d]furan-5,10-dione, a novel metabolite isolated from Crescentia cujete

The title natural product 1, which possesses a new ring skeleton, has been synthesised by a sequence in which the key steps involve a tandem intramolecular Diels-Alder/reverse Diels-Alder reaction sequence. Thus 3-(2-furyl)-1,4-dimethoxynaphthalen-2-ol wa

α1-Adrenoceptor agonists: The identification of novel α1A subtype selective 2′-heteroaryl-2-(phenoxymethyl)imidazolines

Novel 2′-heteroaryl-2-(phenoxymethyl)imidazolines have been identified as potent agonists of the cloned human α1-adrenoceptors in vitro. The nature of the 2′-heteroaryl group can have significant effects on the potency, efficacy, and subtype selectivity in this series. α1A Subtype selective agonists have been identified.

Chromium- and tungsten-triggered valence isomerism of cis-1-acyl-2-ethynylcyclopropanes via [3,3] sigmatropy of (2-acylcyclopropyl)vinylidene - Metal intermediates

The reaction of cis vicinal acetylethynylcyclopropanes 1 with a catalytic amount of M(CO)5(THF) (M = Cr or W) in the presence of Et3N at room temperature gave ortho-substituted phenols 7 in good yields as valence isomerized products. In the absence of Et3N the reactions did not work at all. The reaction of a cyclopropane having an ester or an amide instead of an acetyl moiety with M(CO)5(THF) did not take place, whereas an ethynylvinylcyclopropane gave a mixture of 1- and 2-substituted 1,3,5-cycloheptatrienes. These valence isomerization reactions are assumed to proceed via the formation of vinylidene-metal intermediates 2 from terminal alkynyl moieties followed by [3,3]sigmatropy of 2 to give seven-membered carbene complexes 3. Copyright

REARRANGEMENT OF 2-HETARYLALKYLPYRIDINIUM SALTS

The rearrangement of 2-thienyl- and 2-furylalkylpyridinium salts to the corresponding anilines by the action of methylammonium sulfites has been studied.It has been shown that the rearrangement of these salts is accompanied in many cases by the formation of phenols and dealkylation products.The influence of the length of the alkyl chain between the heterocyclic rings on the ratio of the rearrangement products has been investigated.