5322-56-5

Usage

Structure

Benzene ring with a fluorine atom at the 4-position
Thiol group at the 1-position
Three-carbon chain with a chlorine substituent attached to the thiol group

Applications

Building block for the synthesis of other organic compounds
Used in pharmaceutical, agriculture, and materials industries

Reactivity

Properties and reactivity make it suitable for various chemical reactions and processes

Safety

Important to handle with care
May be hazardous if not used properly

Functional groups

Fluorine atom
Thiol group
Chlorine substituent

Physical state

Likely a liquid or solid at room temperature (not specified in the material)

Chemical properties

May undergo substitution, addition, or elimination reactions due to the presence of the thiol group and chlorine substituent

Stability

Stability may vary depending on reaction conditions and the presence of other reagents

Purity

Purity may affect its reactivity and suitability for specific applications

Storage

Should be stored in a cool, dry, and well-ventilated area, away from incompatible substances

Disposal

Proper disposal methods should be followed to minimize environmental impact and safety hazards

Regulatory information

May be subject to specific regulations and guidelines depending on the region and intended use

Suppliers

Can be obtained from various chemical suppliers or manufacturers specializing in organic compounds
Please note that some properties, such as physical state, stability, and purity, are not explicitly mentioned in the provided material. The information listed above is inferred based on the general knowledge of chemical compounds with similar structures and functional groups.

Upstream product

• 371-42-6 4-Fluorothiophenol 
• 109-70-6 1.3-chlorobromopropane 

Downstream Products

• 55717-04-9 3-CHLOROPROPYL 4-FLUOROPHENYL SULFOXIDE 
• 141891-68-1 1,4-dioxa-8-[3-[(4-fluorophenyl)thio]propyl]-8-azaspiro[4,5]decane 

Relevant academic research and scientific papers

Increasing Complexity: A Practical Synthetic Approach to Three-Dimensional, Cyclic Sulfoximines and First Insights into Their in Vitro Properties

A short synthetic approach with broad scope to access five- to seven-membered cyclic sulfoximines in only two to three steps from readily available thiophenols is reported. Thus, simple building blocks were converted to complex molecular structures by a s

Further evaluation of the tropane analogs of haloperidol

Previous work from our labs has indicated that a tropane analog of haloperidol with potent D2 binding but designed to avoid the formation of MPP+-like metabolites, such as 4-(4-chlorophenyl)-1-(4- (4-fluorophenyl)-4-oxobutyl)pyridin-

Synthesis and QSAR studies on hypotensive 1-[3-(4-substituted phenylthio) propyl]-4-(substituted phenyl) piperazines

A series of 1-[3-(4-substituted phenylthio) propyl]-4-(substituted phenyl) piperazines has been synthesized and evaluated for hypotensive activity. The QSAR studies indicate that resonance and hydrophobic parameters of the aryl substituents are important

5-HT7 receptor antagonists

The present invention relates to compounds having pharmacological activity toward the 5-HT7receptor. Pharmaceutical compositions and methods for their use in the treatment of CNS disorders are described.

Substituted thiazolyl and substituted pyridinyl derivatives

Substituted thiazolyl and substituted pyridinyl derivatives of formula STR1 the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein --A1 =A2 --A3 =A4 -- is a

Central nervous system antiischemic agents

A series of phenylalkylaminoalkyl derivatives of Formula I wherein Ar is naphtyl or phenyl; R1 is hydrogen, fluoro or R?CONH-; R2 is hydrogen or C?-? alkyl; R? is C?-? alkyl; R? is C?-? alkyl or phenyl-C?- ? alkyl; x is zero or the integers 1 and 2; m is