1462-96-0

Basic information

• Product Name: 1-Ethylcyclopentanol
• Synonyms: 1-ETHYLCYCLOPENTANOL;1-ETHYL-1-CYCLOPENTANOL;1-Ethylcyclopentane-1-ol;1-ethylcyclopentan-1-ol;1-Ethyl-1-hydroxycyclopentane
• CAS NO: 1462-96-0
• Molecular Formula: C₇H₁₄O
• Molecular Weight: 114.19
• EINECS: 1312995-182-4
• Product Categories: fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis
• Mol File: 1462-96-0.mol
• Article Data: 12

Chemical Properties

• Melting Point: -10°C(lit.)
• Boiling Point: 153°C(lit.)
• Flash Point: 49°(120°F)
• Appearance: Colorless to yellow/Liquid
• Density: 0.909 g/mL at 25 °C
• Vapor Pressure: 0.73mmHg at 25°C
• Refractive Index: 1.4570
• Storage Temp.: 2-8°C
• PKA: 15.38±0.20(Predicted)
• Sensitive: Moisture Sensitive
• CAS DataBase Reference: 1-Ethylcyclopentanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Ethylcyclopentanol(1462-96-0)
• EPA Substance Registry System: 1-Ethylcyclopentanol(1462-96-0)

Safety Data

• Hazard Codes: Xn
• Statements: 10-22-36
• Safety Statements: 26
• RIDADR: UN 1993C 3 / PGIII
• WGK Germany: 3
• HazardClass: 3
• PackingGroup: III
• Hazardous Substances Data: 1462-96-0(Hazardous Substances Data)

Usage

General Description

1-Ethylcyclopentanol is a chemical compound with the molecular formula C8H16O. It is a colorless liquid with a minty and floral odor, and it is commonly used as a flavoring agent and fragrance in various consumer products. 1-Ethylcyclopentanol is mainly used in the production of perfumes, soaps, and cosmetics due to its pleasant aroma. It is also used as a solvent in the manufacturing of plastics, resins, and pharmaceuticals. Additionally, it can be used as an intermediate in the synthesis of other organic compounds. While 1-Ethylcyclopentanol is generally considered to have low toxicity, prolonged exposure to high concentrations may cause irritation to the skin, eyes, and respiratory system.

InChI:InChI=1/C7H14O/c1-2-6-4-3-5-7(6)8/h6-8H,2-5H2,1H3

Upstream product

• 10467-10-4 ethylmagnesium iodide 
• 120-92-3 cyclopentanone 
• 925-90-6 ethylmagnesium bromide 
• 811-49-4 ethyllithium 
• 17356-19-3 1-ethynylcyclopentanol 
• 19873-00-8 1-Chlor-1-ethylcyclopentan 
• 14660-52-7 ethyl 5-bromovalerate 
• 38118-79-5 1-cyclopentylethan-1-amine 
• 7782-77-6 cis-nitrous acid 
• 2386-64-3 ethylmagnesium chloride 
• 75-03-6 ethyl iodide 
• 2015-57-8 1-benzylcyclopentanol 
• 97-94-9 triethyl borane 

Downstream Products

• 2146-38-5 1-ethylcyclopentene 
• 2146-37-4 ethylidenecyclopentane 
• 55631-69-1 4-(1-ethyl-cyclopentyl)-phenol 
• 2565-39-1 hept-6-en-3-one 
• 31849-01-1 δ-chlorobutyl ethyl ketone 
• 2955-59-1 3,12-tetradecanedione 
• 106-35-4 heptan-3-one 
• 120-92-3 cyclopentanone 
• 3742-80-1 1-ethylcyclopentyl acetate 
• 431-03-8 dimethylglyoxal 
• 2931-10-4 2-ethylcyclopent-2-en-1-one 
• 92104-68-2 1-Ethyl-1-phenyl-cyclopentan 
• 3896-31-9 1-Ethyl-1-acetamido-cyclopentan 
• 3301-90-4 6-ethyl-tetrahydro-2H-pyran-2-one 

Relevant articles and documents

ETHERS AND ESTERS OF 1-SUBSTITUTED CYCLOALKANOLS FOR USE AS AROMA CHEMICALS

The present invention relates to the use of an ether or an ester of a 1 -substituted cycloalkanol or of mixtures of two or more ethers or esters of 1 -substituted cycloalkanols or of a stereoisomer thereof or of a mixture of two or more stereoisomers thereof as aroma chemicals; to the use thereof for modifying the scent character of a fragranced composition; to an aroma chemical composition containing an ether or an ester of a 1 -substituted cycloalkanol or of mixtures of two or more ethers or esters of 1 -substituted cycloalkanols or of a stereoisomer thereof or of a mixture of two or more stereoisomers thereof; and to a method of preparing a fragranced composition or for modifying the scent character of a fragranced composition. The invention further relates to specific ethers or esters of 1 -substituted cycloalkanols.

Carbon Dioxide as a Directing Group for C-H Functionalization Reactions Involving Lewis Basic Amines, Alcohols, Thiols, and Phosphines for the Synthesis of Compounds

Methods of synthesizing compounds using CO2 as a directing group for C—H functionalization, and compounds made thereby, are described.

Photolysis of 1-alkylcycloalkanols in the presence of (diacetoxyiodo) benzene and I2. Intramolecular selectivity in the β-scission reactions of the intermediate 1-alkylcycloalkoxyl radicals

The C-C β-scission reactions of 1-alkylcycloalkoxyl radicals, generated photochemically by visible light irradiation of CH2Cl 2 solutions containing the parent 1-alkylcycloalkanols, (diacetoxy)-iodobenzene (DIB), and I2, have been investigated through the analysis of the reaction products. The 1-alkylcycloalkoxyl radicals undergo competition between ring opening and C-alkyl bond cleavage as a function of ring size and of the nature of the alkyl substituent. With the 1-propylcycloheptoxyl, 1-propylcyclooctoxyl, and 1-phenylcyclooctoxyl radicals, formation of products deriving from an intramolecular 1,5-hydrogen atom abstraction reaction from the cycloalkane ring has also been observed. The results are discussed in terms of release of ring strain associated to ring opening, stability of the alkyl radical formed by C-alkyl cleavage, and with cycloheptoxyl and cyclooctoxyl radicals, also in terms of the possibility of achieving a favorable geometry for intramolecular hydrogen atom abstraction.