17481-19-5

Basic information

• Product Name: 3-CHLORO-1-PROPANETHIOL
• Synonyms: 3-CHLOROPROPANETHIOL;3-CHLORO-1-PROPANETHIOL;1-Propanethiol, 3-chloro-;3-Chloropropane-1-thiol;Einecs 241-496-0;3-Chloropropan-1-thiol;3-Chloro-1-propanethiol 98%
• CAS NO: 17481-19-5
• Molecular Formula: C₃H₇ClS
• Molecular Weight: 110.61
• EINECS: 241-496-0
• Product Categories: Self Assembly&Contact Printing;Self-Assembly Materials;Sulfur Compounds;Thiols/Mercaptans;ThiolsOrganic Building Blocks
• Mol File: 17481-19-5.mol

Chemical Properties

• Boiling Point: 145.5 °C(lit.)
• Flash Point: 110 °F
• Appearance: /
• Density: 1.136 g/mL at 25 °C(lit.)
• Vapor Pressure: 5.02mmHg at 25°C
• Refractive Index: n20/D 1.4921(lit.)
• PKA: 10.04±0.10(Predicted)
• CAS DataBase Reference: 3-CHLORO-1-PROPANETHIOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLORO-1-PROPANETHIOL(17481-19-5)
• EPA Substance Registry System: 3-CHLORO-1-PROPANETHIOL(17481-19-5)

Safety Data

• Hazard Codes: Xi
• Statements: 10-36/37/38
• Safety Statements: 16-26-36/37/39
• RIDADR: UN 3336 3/PG 2
• WGK Germany: 3
• HazardClass: 3.2
• PackingGroup: III
• Hazardous Substances Data: 17481-19-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-1-propanethiol is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of complex organic molecules. Its structural similarity to propanethiol allows for the creation of novel compounds with potential therapeutic applications.
Used in Organic Synthesis:
3-Chloro-1-propanethiol is used as a reagent in organic synthesis for its ability to react with other compounds to form a wide range of products. Its chlorine atom can participate in various chemical reactions, making it a valuable component in the synthesis of new organic compounds.
Used in Research and Development:
3-Chloro-1-propanethiol is used as a research compound in the development of new chemical processes and understanding the properties of organosulfur compounds. Its unique structure and reactivity provide insights into the behavior of similar compounds and their potential applications in various fields.

InChI:InChI=1/C3H7ClS/c4-2-1-3-5/h5H,1-3H2

Upstream product

• 109-70-6 1.3-chlorobromopropane 
• 13012-54-9 thioacetic acid S-(3-chloropropyl) ester 

Downstream Products

• 25850-55-9 1-((4-chlorophenylthio)(phenyl)methylthio)-4-chlorobenzene 
• 1379616-98-4 benzhydryl (3-chloropropyl)sulphane 
• 1480593-49-4 4,5-bis-(3-chloropropylsulfanyl)phthalonitrile 
• 1429333-40-3 2-(4-methoxyphenylimino)-1,3-thiaselenane 
• 1429333-52-7 3-(4-methoxyphenyl)-1,3-thiazinane-2-selenone 
• 1429333-41-4 2-(4-methoxyphenylimino)-1,3-thiaselenane 
• 1429333-38-9 2-(4-chlorophenylimino)-1,3-thiaselenane 
• 1429333-51-6 3-(4-chlorophenyl)-1,3-thiazinane-2-selenone 
• 1429333-39-0 2-(4-chlorophenylimino)-1,3-thiaselenane 
• 1429333-36-7 2-(2-methylphenylimino)-1,3-thiaselenane 
• 1429333-50-5 3-(2-methylphenyl)-1,3-thiazinane-2-selenone 
• 1429333-37-8 2-(2-methylphenylimino)-1,3-thiaselenane 
• 1429333-34-5 2-(4-methylphenylimino)-1,3-thiaselenane 
• 1429333-49-2 3-(4-methylphenyl)-1,3-thiazinane-2-selenone 

Relevant articles and documents

A general and mild synthesis of thioesters and thiols from halides

The conversion of a wide variety of halides to thioesters by reaction with potassium thiocetate under mild conditions is described, and the generality of the method is demonstrated.