164334-74-1

Basic information

• Product Name: 3-(4-FLUOROPHENYL)BENZALDEHYDE
• Synonyms: 3-(4-FLUOROPHENYL)BENZALDEHYDE;AKOS BAR-0062;TIMTEC-BB SBB010233;4'-Fluorobiphenyl-3-carboxaldehyde;4'-FLUOROBIPHENYL-3-CARBALDEHYDE;4'-FLUORO[1,1'-BIPHENYL]-3-CARBALDEHYDE;4'-FLUORO-[1,1'-BIPHENYL]-3-CARBOXALDEHYDE
• CAS NO: 164334-74-1
• Molecular Formula: C₁₃H₉FO
• Molecular Weight: 200.21
• Product Categories: pharmacetical
• Mol File: 164334-74-1.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 328.8 °C at 760 mmHg
• Flash Point: 221.3 °C
• Appearance: /
• Density: 1.173 g/cm³
• Vapor Pressure: 0.000185mmHg at 25°C
• Refractive Index: 1.59
• CAS DataBase Reference: 3-(4-FLUOROPHENYL)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-FLUOROPHENYL)BENZALDEHYDE(164334-74-1)
• EPA Substance Registry System: 3-(4-FLUOROPHENYL)BENZALDEHYDE(164334-74-1)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-41-22
• Safety Statements: 26-36/37/39-39
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 164334-74-1(Hazardous Substances Data)

Usage

General Description

3-(4-Fluorophenyl)benzaldehyde is a chemical compound with the molecular formula C13H9FO. It is an aromatic compound that consists of a benzene ring with a fluorine-substituted phenyl group and an aldehyde functional group. 3-(4-FLUOROPHENYL)BENZALDEHYDE is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds. It is also used in the production of dyes, perfumes, and flavorings. 3-(4-Fluorophenyl)benzaldehyde has potential applications in the fields of medicine, agriculture, and chemical industry due to its versatile reactivity and valuable properties.

InChI:InChI=1/C13H9FO/c14-13-6-4-11(5-7-13)12-3-1-2-10(8-12)9-15/h1-9H

Upstream product

• 591-24-2 3-Methylcyclohexanone 
• 24654-55-5 trans-4-fluorocinnamaldehyde 
• 1765-93-1 4-fluoroboronic acid 
• 3132-99-8 m-bromobenzoic aldehyde 
• 10540-44-0 4'-fluoro-3-methyl-1,1'-biphenyl 
• 352-34-1 4-fluoro-1-iodobenzene 
• 13002-99-8 3-Dibromomethyl-4'-fluorobiphenyl 

Downstream Products

• 10540-39-3 4’-fluoro-[1,1’-biphenyl]-3-carboxylic acid 
• 1367349-44-7 (E)-3-(4'-fluoro-[1,1'-biphenyl]-3-yl)-1-(4-fluorophenyl)prop-2-en-1-one 
• 1367349-45-8 (E)-3-(4'-fluoro-[1,1'-biphenyl]-3-yl)-1-(4-hydroxyphenyl)prop-2-en-1-one 
• 773871-79-7 (4′-fluoro-[1,1′-biphenyl]-3-yl)methanol 

Relevant articles and documents

Microwave-assisted organic acid-base-co-catalyzed tandem Meinwald rearrangement and annulation of styrylepoxides

A novel organic acid-base-co-catalyzed conversion of styrylepoxides into [1,1′-biaryl]-3-carbaldehydes was realized under microwave irradiation. Styrylepoxides first underwent an acid-catalyzed Meinwald rearrangement followed by a tandem base-catalyzed Michael addition, aldol addition, and aromatization sequence to generate [1,1′-biaryl]-3-carbaldehydes.

4-Aryliden-2-methyloxazol-5(4H)-one as a new scaffold for selective reversible MAGL inhibitors

This study reports on a preliminary structure-activity relationship exploration of 4-aryliden-2-methyloxazol-5(4H)-one-based compounds as MAGL/FAAH inhibitors. Our results highlight that this scaffold may serve for the development of selective MAGL inhibi

GLUCOSYLCERAMIDE SYNTHASE INHIBITORS FOR THE TREATMENT OF DISEASES

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions associated with the enzyme glucosylceramide synthase (GCS).