36866-66-7

Basic information

• Product Name: 2-Furanol, tetrahydro-5-phenyl-
• CAS NO: 36866-66-7
• Molecular Formula: C10H12O2
• Molecular Weight: 164.204
• Mol File: 36866-66-7.mol
• Article Data: 32

Chemical Properties

• CAS DataBase Reference: 2-Furanol, tetrahydro-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furanol, tetrahydro-5-phenyl-(36866-66-7)
• EPA Substance Registry System: 2-Furanol, tetrahydro-5-phenyl-(36866-66-7)

Safety Data

• Hazardous Substances Data: 36866-66-7(Hazardous Substances Data)

Usage

Description

2-Furanol, tetrahydro-5-phenylis a chemical compound with a molecular formula C10H12O2. It is a colorless to pale yellow liquid with a strong odor. 2-Furanol, tetrahydro-5-phenylis known for its sweet, caramel-like aroma and taste, and it is commonly used in the food and beverage industry as a flavoring agent. Additionally, it is utilized as a fragrance ingredient in perfumes and cosmetics. 2-Furanol, tetrahydro-5-phenylhas also been studied for its potential biological and pharmacological properties, such as antimicrobial and antioxidant activities. However, it is crucial to handle and use this chemical with caution due to its potential hazardous effects on human health and the environment.

Uses

Used in Food and Beverage Industry:
2-Furanol, tetrahydro-5-phenylis used as a flavoring agent for its sweet, caramel-like aroma and taste, enhancing the flavor profiles of various food and beverage products.
Used in Perfumes and Cosmetics:
2-Furanol, tetrahydro-5-phenylis used as a fragrance ingredient in perfumes and cosmetics, contributing to the creation of pleasant and long-lasting scents.
Used in Pharmaceutical and Biotechnology Research:
2-Furanol, tetrahydro-5-phenylis studied for its potential biological and pharmacological properties, such as antimicrobial and antioxidant activities, which may lead to the development of new drugs and therapies.

Upstream product

• 1008-76-0 4,5-dihydro-5-phenyl-2(3H)-furanone 
• 119135-31-8 (E)-1-phenyl-4-isopropoxydimethylsilyl-3-buten-1-ol O-trimethylsilyl ether 
• 104824-00-2 5-phenyl-2-trimethylsilyl-4,5-dihydrofuran 
• 244168-29-4 N-methoxy-N-methyl-4-oxo-4-phenylbutanamide 
• 622860-41-7 trans-1,5-diphenyl-4-penten-1-ol 
• 201230-82-2 carbon monoxide 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 2051-95-8 succinylbenzene 
• 638-37-9 butanedial 
• 591-51-5 phenyllithium 
• 50-00-0 formaldehyd 
• 1229893-66-6 (Z)-4-hydroxy-4-phenylbut-1-enyl acetate 
• 102632-99-5 1-phenyl-4-penten-1-ol 
• 4850-50-4 1-phenyl-butane-1,4-diol 

Downstream Products

• 83268-77-3 6-phenyl-2,2-(trimethylenedithio)tetrahydropyran 
• 1187461-93-3 (E)-5-cyclopropyl-1-phenylpent-4-en-1-ol 
• 1187461-79-5 (E)-methyl 6-hydroxy-6-phenylhex-2-enoate 

Relevant articles and documents

Cobalt-catalysed addition of allylidene dipivalate to aldehydes. A formal homoaldol condensation

A Co(I)-catalysed condensation of allylidene dipivalate with aldehydes to give (Z)-4-hydroxybut-1-enyl pivalates in 62 to 87% isolated yields, is reported. Reactions are run in acetonitrile at 0 or 25°C depending on the nature of the aldehyde, and exploit

Selective mono addition of aryllithiums to dialdehydes by micromixing

Micromixing enables highly selective mono addition of aryllithiums to dialdehydes. Because the unchanged formyl group in the products can be used for further transformations, the present approach serves as a powerful method for protecting-group-free synthesis.

Unusual aluminum hydride-mediated reduction of N-(γ- or δ-oxoacyl)oxazolidinone

Reduction of N-(γ-oxoacyl)oxazolidinone with a borohydride reagent, such as NaBH4 or LiBEt3H, resulted in formation of the corresponding lactone or lactol. In contrast, when an aluminum hydride reagent was used instead of a borohydride reagent, reduction of N-(γ- or δ-oxoacyl)oxazolidinone proceeded unexpectedly to give not the corresponding lactone or lactol, but a tetrahydrofuran or tetrahydropyran derivative, respectively, containing an oxazolidino group.

Microwave-assisted domino hydroformylation without syngas

Hydroformylation is a powerful reaction that has suffered for some negative prejudices related to the use of gaseous H2 and CO. Now it is possible to carry out hydroformylation and different cyclohydrocarbonylations, even on complex substrates, using aqueous formalin as H2 and CO surrogate in few minutes under microwave irradiation. The catalytic system developed by Morimoto (Rh/BINAP for decomposition of formaldehyde and Rh/Xantphos for hydroformylation) is compatible with microwave dielectric heating and with complex substrates containing ligand atoms allowing rapid domino hydroformylation cyclization reactions without using the external supply of gaseous H2 and CO (gas cylinder) and without any particular safety limitation or device. Georg Thieme Verlag Stuttgart.