trans-1-(Phenylthio)-2-butene

Base Information

Chemical Name:trans-1-(Phenylthio)-2-butene
CAS No.:36195-56-9
Molecular Formula:C10H12S
Molecular Weight:164.271
Hs Code.:
Nikkaji Number:J1.174.398F,J846.609B
Mol file:36195-56-9.mol

Synonyms:trans-1-(Phenylthio)-2-butene;36195-56-9;CROTYL PHENYL SULFIDE;Crotylphenyl sulfide;Phenyl(2-butenyl) sulfide;SCHEMBL8649390;[(E)-but-2-enyl]sulfanyl-benzene;AKOS024324284

Suppliers and Price of trans-1-(Phenylthio)-2-butene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of trans-1-(Phenylthio)-2-butene

Chemical Property:

Vapor Pressure:0.0941mmHg at 25°C
Boiling Point:231.5°Cat760mmHg
Flash Point:92.4°C
Density:1g/cm³
XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:164.06597156
Heavy Atom Count:11
Complexity:112

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC=CCSC1=CC=CC=C1
Isomeric SMILES:C/C=C/CSC1=CC=CC=C1

Technology Process of trans-1-(Phenylthio)-2-butene

There total 24 articles about trans-1-(Phenylthio)-2-butene 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: 96.0%

: 4784-77-4,39616-19-8,29576-14-5
(E)-1-Bromo-2-butene

: 108-98-5
thiophenol

: 701-75-7
3-(phenylthio)but-1-ene

: 36195-55-8
(Z)-but-2-en-1-yl phenyl sulfide

: 36195-56-9
(E)-but-2-en-1-yl phenyl sulfide

Guidance literature:: With sodium methylate; In methanol; Yields of byproduct given. Title compound not separated from byproducts; 0 deg C, 1 h; 25 deg C, overnight;
DOI:10.1246/bcsj.57.2781

Reference yield: 95.0%

: 504-61-0,542-72-3
(E)-but-2-enol

: 108-98-5
thiophenol

: 36195-56-9
(E)-but-2-en-1-yl phenyl sulfide

Guidance literature:: With bis(2,2,2-trifluoroethoxy)triphenylphosphorane; In diethyl ether; dichloromethane; for 20h;
DOI:10.1021/jo01313a008