5323-03-5

Basic information

• Product Name: 1-[(2-CHLOROETHYL)THIO]-4-FLUOROBENZENE
• Synonyms: 1-(2-chloroethylsulfanyl)-4-fluorobenzene
• CAS NO: 5323-03-5
• Molecular Formula: C₈H₈ClFS
• Molecular Weight: 0
• Mol File: 5323-03-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.53g/cm³
• Vapor Pressure: 0.04mmHg at 25°C
• Refractive Index: 1.551
• CAS DataBase Reference: 1-[(2-CHLOROETHYL)THIO]-4-FLUOROBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[(2-CHLOROETHYL)THIO]-4-FLUOROBENZENE(5323-03-5)
• EPA Substance Registry System: 1-[(2-CHLOROETHYL)THIO]-4-FLUOROBENZENE(5323-03-5)

Safety Data

• Hazardous Substances Data: 5323-03-5(Hazardous Substances Data)

Usage

Physical state

Colorless liquid

Odor

Strong

Uses

a. Reagent in organic synthesis
b. Precursor to various aromatic compounds
c. Intermediate in the production of agrochemicals and pharmaceuticals

Hazardous nature

Considered hazardous to human health and the environment

Handling precautions

Handle with caution

InChI:InChI=1/C8H8ClFS/c9-5-6-11-8-3-1-7(10)2-4-8/h1-4H,5-6H2

Upstream product

• 5322-63-4 2-[(4-fluorophenyl)thio]ethanol 
• 371-42-6 4-Fluorothiophenol 
• 107-06-2 1,2-dichloro-ethane 

Downstream Products

• 28122-12-5 1-(2-chloro-ethanesulfinyl)-4-fluoro-benzene 
• 70931-42-9 1-<2-(4-fluorophenylthio)ethyl>piperazine 

Relevant articles and documents

SUBSTITUTED NICOTINAMIDE COMPOUNDS AND USES THEREOF

Substituted nicotinamide compounds corresponding to formula I a process for their preparation, pharmaceutical compositions containing these compounds, and the use thereof for the treatment or inhibition conditions such as pain, epilepsy, migraine, anxiety states, or urinary incontinence.

2-imino-6-polyfluoroalkoxybenzothiazole derivatives, and pharamaceutical compositions containing them and their treatment of medical conditions associated with the effects of glutamate

Compounds of formula: STR1 and their salts, in which R1 represents polyfluoroalkoxy, and R2 represents alkyl, alkenyl (3-6 C), [cycloalkyl (3-6 C)]-alkyl, carbamoylalkyl, dialkylcarbamoylalkyl, acylaminoalkyl, phenylthioalkyl, hydroxyalkyl, cyanoalkyl, sulphamoylethyl, N-alkylsulphamoylethyl, pyridylthioalkyl, pyridiylalkylthioalkyl, pyridylsulphinylalkyl, alkynyl (3-6 C), phenylsulphinylalkyl, halophenylthioalkyl, (2,2,2-trifluoroethylthio)alkyl, 2-dialkylaminopropyl, pyrimidinylsulphinylalkyl, pyridylalkylsulphinylalkyl, halophenylsulphinylalkyl or (2,2,2-trifluoroethylsulphinyl)alkyl are useful in the treatment of medical conditions associated with the effects of glutamate.