Allyl methyl trisulfide

Base Information

• Chemical Name: Allyl methyl trisulfide
• CAS No.: 34135-85-8
• Molecular Formula: C4H8S3
• Molecular Weight: 152.306
• Hs Code.: 2930909090
• European Community (EC) Number: 251-843-8
• UNII: 983O8ZL28A
• DSSTox Substance ID: DTXSID30187717
• Nikkaji Number: J132.895F
• Wikidata: Q27272080
• Metabolomics Workbench ID: 46532
• Mol file: 34135-85-8.mol

Synonyms:allyl methyl trisulfide;MATS;methyl allyl trisulphide;methylallyl trisulfide;trisulfide methyl 2-propenyl

Chemical Property of Allyl methyl trisulfide

Chemical Property:

• Appearance/Colour: Yellow liquid.
• Vapor Pressure: 0.249mmHg at 25°C
• Melting Point: < 25oC
• Refractive Index: 1.588
• Boiling Point: 212.678 °C at 760 mmHg
• Flash Point: 82.907 °C
• PSA: 75.90000
• Density: 1.1578 g/cm³
• LogP: 2.83180
• XLogP3: 2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 151.97881378
• Heavy Atom Count: 7
• Complexity: 44.2

Purity/Quality:

99% ^*data from raw suppliers

Methylallyltrisulfide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CSSSCC=C
• Uses: Methyl allyl trisulfide is a volatile organic compound, and a component of the essential oils of garlic (Allium sativum L.). Methyl allyl trisulfide shows antiviral activity against HSV-1 in African green monkey kidney cell and antioxidant activity against DPPH radical in DMSO.

Technology Process of Allyl methyl trisulfide

There total 1 articles about Allyl methyl trisulfide 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: 60.0%

prop-2-ene-1-thiol (870-23-5) + Methoxycarbonylmethyl trisulfane (94839-60-8) → Methyl 2-propenyl trisulfane (34135-85-8)

Guidance literature:

4-methyl-morpholine; In chloroform; at 25 ℃; for 16h;

DOI:10.1055/s-1984-30922

upstream raw materials:

prop-2-ene-1-thiol

Methoxycarbonylmethyl trisulfane

Refernces