(2-Methylcyclopent-2-en-1-yl)sulfanylbenzene

Base Information

Chemical Name:(2-Methylcyclopent-2-en-1-yl)sulfanylbenzene
CAS No.:104301-66-8
Molecular Formula:C₁₂H₁₄S
Molecular Weight:190.309
Hs Code.:
DSSTox Substance ID:DTXSID701264747

Synonyms:104301-66-8;DTXSID701264747;[(2-Methyl-2-cyclopenten-1-yl)thio]benzene

Suppliers and Price of (2-Methylcyclopent-2-en-1-yl)sulfanylbenzene

Supply Marketing:

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

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Chemical Property of (2-Methylcyclopent-2-en-1-yl)sulfanylbenzene

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:190.08162162
Heavy Atom Count:13
Complexity:189

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CCCC1SC2=CC=CC=C2

Technology Process of (2-Methylcyclopent-2-en-1-yl)sulfanylbenzene

There total 5 articles about (2-Methylcyclopent-2-en-1-yl)sulfanylbenzene 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:

: 52190-40-6
2-(phenylthio)cyclopentanone

: 104301-66-8
1-Methyl-5-phenylthiocyclopent-1-ene

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / KH

2: 1.) LiALH₄ / 2.) toluene-p-sulphonic acid / 1.) Et₂O, 0 gradC 2.) benzene, reflux, 15 min

With lithium aluminium tetrahydride; potassium hydride; toluene-4-sulfonic acid;
DOI:10.1016/S0040-4039(00)84095-2

Reference yield:

: 930-69-8
sodium thiophenolate

: 104301-66-8
1-Methyl-5-phenylthiocyclopent-1-ene

Guidance literature:: Multi-step reaction with 3 steps

2: 70 percent / KH

3: 1.) LiALH₄ / 2.) toluene-p-sulphonic acid / 1.) Et₂O, 0 gradC 2.) benzene, reflux, 15 min

With lithium aluminium tetrahydride; potassium hydride; toluene-4-sulfonic acid;
DOI:10.1016/S0040-4039(00)84095-2

Reference yield:

: 120-92-3
cyclopentanone

: 104301-66-8
1-Methyl-5-phenylthiocyclopent-1-ene

Guidance literature:: Multi-step reaction with 3 steps

2: 70 percent / KH

3: 1.) LiALH₄ / 2.) toluene-p-sulphonic acid / 1.) Et₂O, 0 gradC 2.) benzene, reflux, 15 min

With lithium aluminium tetrahydride; potassium hydride; toluene-4-sulfonic acid;
DOI:10.1016/S0040-4039(00)84095-2