ETHYL N-PROPYL SULFIDE

Base Information

• Chemical Name: ETHYL N-PROPYL SULFIDE
• CAS No.: 4110-50-3
• Molecular Formula: C5H12S
• Molecular Weight: 104.216
• Hs Code.: 2930909090
• European Community (EC) Number: 223-890-4
• NSC Number: 163319
• UNII: 4FK48S87VH
• DSSTox Substance ID: DTXSID3041958
• Nikkaji Number: J44.105H
• Wikidata: Q27259528
• Mol file: 4110-50-3.mol

Synonyms:Sulfide,ethyl propyl (6CI,7CI,8CI);1-(Ethylthio)propane;3-Thiahexane;Ethyl n-propylsulfide;Ethyl propyl sulfide;Ethyl propyl thio ether;NSC 163319;Propylethyl sulfide;

Chemical Property of ETHYL N-PROPYL SULFIDE

Chemical Property:

• Vapor Pressure: 0.012mmHg at 25°C
• Melting Point: -117°C
• Refractive Index: 1.519
• Boiling Point: 120.2 °C at 760 mmHg
• Flash Point: 18.9 °C
• PSA: 25.30000
• Density: 0.833 g/cm³
• LogP: 2.14950
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 104.06597156
• Heavy Atom Count: 6
• Complexity: 19.9

Purity/Quality:

99% ^*data from raw suppliers

Ethyl Propyl Sulfide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): R11:Highly flammable.; R36/37/38:Irritating to eyes, respiratory system and skin.
• Hazard Codes: R11:Highly flammable.; R36/37/38:Irritating to eyes, respiratory system and skin.
• Statements: 11-36/37/38
• Safety Statements: 16-23-26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCSCC

Technology Process of ETHYL N-PROPYL SULFIDE

There total 22 articles about ETHYL N-PROPYL 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:

propene (187737-37-7,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4) + ethanethiol (75-08-1) → ethyl propyl sulfide (4110-50-3)

Guidance literature:

at 100 ℃;

Reference yield:

ethyl bromide (74-96-4) + 1-thiopropane (107-03-9) → ethyl propyl sulfide (4110-50-3)

Guidance literature:

With sodium hydroxide;

DOI:10.1021/ja01152a021

Reference yield:

triethyl phosphite (122-52-1) + Dipropyl disulfide (629-19-6) → ethyl propyl sulfide (4110-50-3)

Guidance literature:

Heating;

DOI:10.1021/ja00894a018

upstream raw materials:

ethyl bromide

1-thiopropane

ascaridole

propene

Downstream raw materials:

propyl ethyl sulfoxide

butyl sulfoxide

ethyl n-propyl sulfone

2-(ethylthio)aniline

Refernces

• 1、 Nesmeyanov, N. A.,Kalyavin, V. A.,Reutov, O. A.. "THE ROLE OF FULLY SUBSTITUTED ORGANOMAGNESIUM COMPOUNDS IN THE REACTION OF ALIPHATIC SULFOXIDES WITH GRIGNARD REAGENTS". . p. 375 - 379. Retrieved 2007/10/02.