59036-45-2

Basic information

• Product Name: {[(2E)-3-chloroprop-2-en-1-yl]sulfanyl}benzene
• CAS NO: 59036-45-2
• Molecular Formula: C₉H₉ClS
• Molecular Weight: 184.6858
• Mol File: 59036-45-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 251.5°C at 760 mmHg
• Flash Point: 105°C
• Density: 1.16g/cm³
• Vapor Pressure: 0.0323mmHg at 25°C
• Refractive Index: 1.589
• CAS DataBase Reference: {[(2E)-3-chloroprop-2-en-1-yl]sulfanyl}benzene(CAS DataBase Reference)
• NIST Chemistry Reference: {[(2E)-3-chloroprop-2-en-1-yl]sulfanyl}benzene(59036-45-2)
• EPA Substance Registry System: {[(2E)-3-chloroprop-2-en-1-yl]sulfanyl}benzene(59036-45-2)

Safety Data

• Hazardous Substances Data: 59036-45-2(Hazardous Substances Data)

Usage

Description

[(2E)-3-chloroprop-2-en-1-yl]sulfanylbenzene is an organosulfur compound characterized by a benzene ring with a thiol group attached to it. It also features a 3-chloroprop-2-ene group, which is a type of olefin. This unique structure and reactivity make it a valuable compound in various chemical applications.

Uses

Used in Organic Synthesis:
[(2E)-3-chloroprop-2-en-1-yl]sulfanylbenzene is used as a building block in organic synthesis for creating more complex organic molecules. Its structural features allow for various chemical reactions, including substitution and addition reactions, making it a versatile component in the synthesis of a wide range of compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [(2E)-3-chloroprop-2-en-1-yl]sulfanylbenzene may be utilized as a starting material or intermediate in the development of new drugs. Its unique structure and reactivity can contribute to the design and synthesis of novel pharmaceutical compounds with potential therapeutic applications.
Used in Agricultural Industry:
[(2E)-3-chloroprop-2-en-1-yl]sulfanylbenzene may also have potential applications in the agricultural industry, where it could be used as a precursor for the development of new agrochemicals, such as pesticides or herbicides. Its unique chemical properties could be harnessed to create more effective and environmentally friendly products for agricultural use.
Overall, the chemical compound [(2E)-3-chloroprop-2-en-1-yl]sulfanylbenzene demonstrates potential usefulness in both laboratory and industrial settings due to its unique structure and reactivity. Its applications span across various fields, including organic synthesis, pharmaceuticals, and agriculture, making it a valuable compound for further research and development.

Upstream product

• 563-57-5 3,3-dichloropropene 
• 930-69-8 sodium thiophenolate 
• 10061-01-5 cis-1,3-Dichloropropene 
• 3223-70-9 chloroallene 
• 108-98-5 thiophenol 
• 64-17-5 ethanol 
• 542-75-6 E/Z-1,3-Dichloropropene 
• 3111-52-2 potassium thiophenolate 
• 882-33-7 diphenyldisulfane 
• 10061-02-6 (E)-1,3-dichloro-prop-1-ene 

Downstream Products

• 877122-44-6 (3t-chloro-allyl)-phenyl sulfone 
• 80780-63-8 (E)-prop-1-ene-1,3-diylbis(phenylsulfane) 
• 58749-54-5 3-chloro-1-(phenylthio)prop-1-ene 

Relevant articles and documents

Effect of chalcogenyl substituent on the course of allyl rearrangement at chalcogenation of 1,3-dichloropropene

Formation of 1,3-dichalcogenylpropene at the treatment of 1,3-dichloropropene with organic dichalcogenides in a redox system hydrazine hydrate–KOH is governed by the possibility of an allyl rearrangement. In the presence of bases this rearrangement proceeds via carbanion partially stabilized by the chalcogenyl substituent. The effectivity of the stabilization and consequently the probability of the rearrangement varies in the series of substituents PhS > BnS > PhSe. In the stage of the direct nucleophilic substitution of chlorine the anion PhSe?possesses the highest activity.