701-38-2

Basic information

• Product Name: 1-(3-FLUOROPHENYL)PROPAN-1-OL
• Synonyms: 1-(3-FLUOROPHENYL)PROPAN-1-OL;1-(3-Fluorophenyl)propanol, 97%;alpha-Ethyl-3-fluorobenzyl alcohol
• CAS NO: 701-38-2
• Molecular Formula: C₉H₁₁FO
• Molecular Weight: 154.18
• Mol File: 701-38-2.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 215.8°C at 760 mmHg
• Flash Point: 104°C
• Appearance: /
• Density: 1.091g/cm³
• Vapor Pressure: 0.0848mmHg at 25°C
• Refractive Index: 1.506
• CAS DataBase Reference: 1-(3-FLUOROPHENYL)PROPAN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-FLUOROPHENYL)PROPAN-1-OL(701-38-2)
• EPA Substance Registry System: 1-(3-FLUOROPHENYL)PROPAN-1-OL(701-38-2)

Safety Data

• Hazardous Substances Data: 701-38-2(Hazardous Substances Data)

Usage

General Description

1-(3-fluorophenyl)propan-1-ol, also known as 3-fluorophenylpropanol or 3-FPM, is a chemical compound with the molecular formula C9H11FO. It is classified as a fluoroalkanol and is used in the manufacturing of pharmaceuticals and fragrance compounds. This chemical is a colorless liquid with a sweet and floral odor. It is commonly used as a building block in organic synthesis and is also known for its potential use as a recreational drug or research chemical. The compound exhibits psychoactive properties, acting as a stimulant and may have implications for use in the field of medicinal chemistry. Additionally, there is research into its potential therapeutic applications, although it has not been approved for medical use in most countries.

InChI:InChI=1/C9H11FO/c1-2-9(11)7-4-3-5-8(10)6-7/h3-6,9,11H,2H2,1H3

Upstream product

• 74-96-4 ethyl bromide 
• 456-48-4 3-Fluorobenzaldehyde 
• 455-67-4 1-(3-fluorophenyl)propan-1-one 
• 1073-06-9 3-fluorobromobenzene 
• 123-38-6 propionaldehyde 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 38340-11-3 1-fluoro-3-(1-propen-1-yl)benzene 
• 28593-12-6 1-(3-fluorophenyl)propane 
• 321939-65-5 2-fluoro-1-iodo-4-propylbenzene 
• 455-67-4 1-(3-fluorophenyl)propan-1-one 
• 172748-78-6 (R)-1-(3-fluoro-phenyl)-propan-1-ol 
• 92821-83-5 2-bromo-1-(3-fluorophenyl)propan-1-one 
• 442661-38-3 4-n-propyl-2-fluorophenylboronic acid 
• 172748-78-6 (S)-1-(3'-fluorophenyl)propan-1-ol 

Relevant articles and documents

Efficient Transfer Hydrogenation of Ketones using Methanol as Liquid Organic Hydrogen Carrier

Herein, we demonstrate an efficient protocol for transfer hydrogenation of ketones using methanol as practical and useful liquid organic hydrogen carrier (LOHC) under Ir(III) catalysis. Various ketones, including electron-rich/electron-poor aromatic ketones, heteroaromatic and aliphatic ketones, have been efficiently reduced into their corresponding alcohols. Chemoselective reduction of ketones was established in the presence of various other reducible functional groups under mild conditions.

Halogen-bonded iodonium ion catalysis: A route to α-hydroxy ketones: Via domino oxidations of secondary alcohols and aliphatic C-H bonds with high selectivity and control

A domino synthesis of α-hydroxy ketones has been developed from benzylic secondary alcohols employing catalytic iodonium ions stabilized by DMSO. The reaction proceeds through an unprecedented sequential oxidation of alcohols to ketone and its α-hydroxylation in a controlled manner. The spectroscopic evidence establishes the possibility of formation of a stable halogen-bonded adduct between DMSO and iodonium ions.

Liquid crystal carbonate and liquid crystal medium containing the same with positive or negative dielectric anisotropy

A novel liquid crystalline carbonate and the mixture containing the same: wherein R3 is an alkyl (H2n+1Cn) or an alkenyl (H2n?1Cn) group, each of 1 to 12 carbon atoms, the ring A is laterally unsubstituted benze