62499-98-3

Basic information

• Product Name: 1-(3-hydroxyprop-1-en-1-yl)cyclohexanol
• CAS NO: 62499-98-3
• Molecular Formula: C₉H₁₆O₂
• Molecular Weight: 156.2221
• Mol File: 62499-98-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 270.8°C at 760 mmHg
• Flash Point: 127.1°C
• Density: 1.154g/cm³
• Vapor Pressure: 0.000876mmHg at 25°C
• Refractive Index: 1.602
• CAS DataBase Reference: 1-(3-hydroxyprop-1-en-1-yl)cyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-hydroxyprop-1-en-1-yl)cyclohexanol(62499-98-3)
• EPA Substance Registry System: 1-(3-hydroxyprop-1-en-1-yl)cyclohexanol(62499-98-3)

Safety Data

• Hazardous Substances Data: 62499-98-3(Hazardous Substances Data)

Usage

Description

1-(3-hydroxyprop-1-en-1-yl)cyclohexanol is a chemical compound with the molecular formula C10H18O2. It is a cyclohexanol derivative featuring a hydroxypropenyl group attached to the cyclohexane ring, known for its unique chemical structure and properties.

Uses

Used in Pharmaceutical Industry:
1-(3-hydroxyprop-1-en-1-yl)cyclohexanol is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to serve as a building block in the development of new drugs, potentially contributing to advancements in medicine.
Used in Fragrance Industry:
In the fragrance industry, 1-(3-hydroxyprop-1-en-1-yl)cyclohexanol is utilized as an ingredient in perfumes and personal care products. Its distinct chemical properties contribute to the creation of diverse and complex scents, enhancing the sensory experience of these products.
Used in Cosmetic Industry:
1-(3-hydroxyprop-1-en-1-yl)cyclohexanol also holds potential applications in the cosmetic industry, where its unique chemical structure and properties can be harnessed for the development of innovative cosmetic products.
Used as a Precursor in Chemical Production:
Furthermore, 1-(3-hydroxyprop-1-en-1-yl)cyclohexanol is employed as a precursor for the production of various other chemicals, highlighting its versatility and importance in the chemical industry.

Upstream product

• 87071-00-9 1-[(E)-3-(Tetrahydro-pyran-2-yloxy)-propenyl]-cyclohexanol 
• 5686-96-4 1-(3-hydroxyprop-1-yn-1-yl)cyclohexan-1-ol 
• 87070-89-1 1-[(Z)-3-(Tetrahydro-pyran-2-yloxy)-1-trimethylsilanyl-propenyl]-cyclohexanol 
• 67-56-1 methanol 
• 78-27-3 1-Ethynylcyclohexan-1-ol 
• 108-94-1 cyclohexanone 

Relevant articles and documents

Atom-Transfer Radical Addition of Alcohols to Aliphatic Alkynes

An intermolecular hydrogen bond-promoted atom-transfer radical addition of simple alcohols to aliphatic alkynes is demonstrated here. Through this strategy, a variety of allyl alcohols can be synthesized in high selectivity and yields. Furthermore, this work reveals the relationship between selectivity and the substrate. ?

Palladium-Catalyzed Carbon Dioxide Elimination-Fixation Reaction of 4-Methoxycarbonyloxy-2-buten-1-ols

A new type of palladium-catalyzed CO2 recycling reaction using allylic carbonates is described. Reaction of trans-4-methoxycarbonyloxy-2-buten-1-ols in the presence of a palladium catalyst produces cyclic carbonates having a vinyl group via a CO2 elimination-fixation process. A variety of allylic carbonates participate in the reaction giving cyclic carbonates with high efficiencies. Stereoselective construction of trans-cyclic carbonates is achieved by using nonsymmetric substrates. An enantiospecific reaction proceeds to give chiral cyclic carbonate when a chiral methyl-substituted substrate is subjected to the reaction conditions.

Stereospecific Synthesis of Hydroxyl-Differentiated (E)- and (Z)-1,4-Enediols

-