Propenyl sulfide

Base Information

• Chemical Name: Propenyl sulfide
• CAS No.: 33922-80-4
• Molecular Formula: C6H10S
• Molecular Weight: 114.211
• Hs Code.: 2930909090
• DSSTox Substance ID: DTXSID10955512
• Mol file: 33922-80-4.mol

Synonyms:propenyl sulfide;1-Propenylsulfanyl-propene;SCHEMBL664383;DTXSID10955512;1-[(Prop-1-en-1-yl)sulfanyl]prop-1-ene

Chemical Property of Propenyl sulfide

Chemical Property:

• Boiling Point: 144.3 °C at 760 mmHg
• Flash Point: 33 °C
• PSA: 25.30000
• Density: 0.886 g/cm³
• LogP: 2.78680
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 114.05032149
• Heavy Atom Count: 7
• Complexity: 62.2

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC=CSC=CC

Technology Process of Propenyl sulfide

There total 4 articles about Propenyl sulfide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

diallyl sulphide (592-88-1) → bis-(1-propenyl) sulfide (33922-80-4) + 1-ethyl-3-isopropylbenzene (4920-99-4)

Guidance literature:

With potassium hydroxide; dimethyl sulfoxide; at 90 ℃; for 5h; Yield given. Yields of byproduct given;

Reference yield:

propionaldehyde (123-38-6) → bis-(1-propenyl) sulfide (33922-80-4)

Guidance literature:

Multistep reaction; (i) HCl, H₂S, (ii) PhNEt₂;

Reference yield:

diallyl sulphide (592-88-1) + sodium ethanolate (141-52-6) → bis-(1-propenyl) sulfide (33922-80-4) + hexa-1,5-diene-3-thiol (245450-14-0)

Guidance literature:

DOI:10.1021/ja01591a063

upstream raw materials:

diallyl sulphide

sodium ethanolate

propionaldehyde

Downstream raw materials:

propyl sulfide

thiophene

2-ethylthiophene

3-methyl-thieno[2,3-b]thiophene