632-02-0

Basic information

• Product Name: 1-CHLORO-3-(TOLENE-P-SULPHONYLOXY) PROPANE
• Synonyms: 3-chloropropyl 4-methylbenzenesulfonate;3-Chloropropylp-toluensulfonate;TOLYL-(3-CHLOROPROPYL)-ETHER;3-CHLOROPROPYL-P-TOLUENESULFONATE;3-CHLOROPROPYLTOSYLATE;1-CHLORO-3-(TOLENE-P-SULPHONYLOXY) PROPANE;4-Methylbenzenesulfonic acid 3-chloropropyl ester
• CAS NO: 632-02-0
• Molecular Formula: C₁₀H₁₃ClO₃S
• Molecular Weight: 248.73
• Mol File: 632-02-0.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 375.6 °C at 760 mmHg
• Flash Point: 181 °C
• Appearance: /
• Density: 1.254 g/cm³
• Vapor Pressure: 1.66E-05mmHg at 25°C
• Refractive Index: 1.524
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-CHLORO-3-(TOLENE-P-SULPHONYLOXY) PROPANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-CHLORO-3-(TOLENE-P-SULPHONYLOXY) PROPANE(632-02-0)
• EPA Substance Registry System: 1-CHLORO-3-(TOLENE-P-SULPHONYLOXY) PROPANE(632-02-0)

Safety Data

• Hazardous Substances Data: 632-02-0(Hazardous Substances Data)

Usage

General Description

1-Chloro-3-(toluene-p-sulphonyloxy) propane, commonly referred to as CTP, is a type of organic compound that contains a chloro group (-Cl), toluene-p-sulphonyloxy group (C6H4(SO3)CH3), and a propyl group (C3H7). This molecule is characterized by its ability to react with a variety of other chemical species because of its chloro and sulphonyloxy functional groups. In the presence of certain catalysts or under specific conditions, these functional groups can undergo a range of chemical reactions such as substitution, elimination, or addition, leading to the formation of new compounds. Its precise applications are dependent on the particular environment or industry but are typically found in fields like organic synthesis or materials chemistry. Always remember to handle chemical substances like CTP with care due to their potential reactivity and hazard risks.

InChI:InChI=1/C10H13ClO3S/c1-9-3-5-10(6-4-9)15(12,13)14-8-2-7-11/h3-6H,2,7-8H2,1H3

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 627-30-5 1-chloro-3-hydroxypropane 

Downstream Products

• 142-28-9 1,3-Dichloropropane 
• 543-59-9 1-Chloropentane 
• 109-70-6 1.3-chlorobromopropane 
• 104-52-9 phenylpropyl chloride 
• 1002-69-3 decyl chloride 
• 5909-59-1 10-(3-chloropropyl)-10H-phenothiazine 
• 114914-08-8 (3-chloro-propyl)-furfuryl sulfide 
• 1124-62-5 3-cyclohexylpropyl chloride 
• 4830-93-7 1-Chloro-4-phenylbutane 
• 92020-95-6 (4-Acetamino-2-acetyl-phenyl)-(3-chlor-propyl)-ether 
• 92656-24-1 <4-Acetamino-2-butyryl-phenyl>-<3-chlor-propyl>-aether 
• 92378-34-2 (5-Propionylamino-2-propionyl-phenyl)-(3-chlor-propyl)-ether 
• 92378-35-3 (4-Acetamino-2-propionyl-phenyl)-(3-chlor-propyl)-ether 
• 97725-98-9 <4-Acetamino-2-isobutyryl-phenyl>-<3-chlor-propyl>-aether 

Relevant articles and documents

Preparation method of optically active N-(halogenated propyl) amino acid derivative

The invention provides a preparation method of an optically active N-(halogenated propyl) amino acid derivative, namely the N-(halogenated propyl) amino acid derivative represented by a formula (I) is obtained by reacting an optically active alanine ester

Development and Kilogram-Scale Synthesis of a D2/5-HT2A Receptor Dual Antagonist (±)-SIPI 6360

The kilogram-scale synthesis of a D2/5-HT2A receptor dual antagonist (±)-SIPI 6360 was developed as an alternative treatment for schizophrenia. Specifically, three conditions were modified and optimized, including the Vilsmeier condi

Efficient synthesis of 1,2-dicyclopropylethyne and (cyclopropylethynyl) cyclobutane from 1,2-di-(ω-haloalkyl)ethynes and 1-cycloalkyl-2-(ω- haloalkyl)ethynes

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