1-(Phenylsulfanyl)cyclopentane-1-carbaldehyde

Base Information

Chemical Name:1-(Phenylsulfanyl)cyclopentane-1-carbaldehyde
CAS No.:115205-40-8
Molecular Formula:C12H14OS
Molecular Weight:206.309
Hs Code.:
DSSTox Substance ID:DTXSID40566478
Nikkaji Number:J677.969G
Wikidata:Q82452103
Mol file:115205-40-8.mol

Synonyms:115205-40-8;1-(Phenylsulfanyl)cyclopentane-1-carbaldehyde;DTXSID40566478

Suppliers and Price of 1-(Phenylsulfanyl)cyclopentane-1-carbaldehyde

Supply Marketing:

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

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Chemical Property of 1-(Phenylsulfanyl)cyclopentane-1-carbaldehyde

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:206.07653624
Heavy Atom Count:14
Complexity:191

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(C1)(C=O)SC2=CC=CC=C2

Technology Process of 1-(Phenylsulfanyl)cyclopentane-1-carbaldehyde

There total 4 articles about 1-(Phenylsulfanyl)cyclopentane-1-carbaldehyde 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: 88.0%

: 115205-37-3
1-(Methoxy-phenylsulfanyl-methyl)-cyclopentanol

: 115205-40-8
1-phenylsulfanylcyclopentane carboxaldehyde

Guidance literature:: With methanesulfonyl chloride; triethylamine; In benzene; at 20 ℃; for 24h;
DOI:10.1021/ja00223a060

Reference yield: 85.0%

: 155091-53-5
1-(diacetoxymethyl)-1-(phenylsulfenyl)cyclopentane

: 115205-40-8
1-phenylsulfanylcyclopentane carboxaldehyde

Guidance literature:: With potassium carbonate; In methanol; at 25 ℃; for 0.333333h;
DOI:10.1016/S0040-4020(01)81812-3

Reference yield:

: 13865-50-4
methoxymethyl phenyl sulfide

: 115205-40-8
1-phenylsulfanylcyclopentane carboxaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-BuLi / tetrahydrofuran

1.2: 80 percent / tetrahydrofuran / -30 °C

2.1: MsCl; Et₃N / benzene / 20 °C

With n-butyllithium; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; benzene;
DOI:10.1021/jo034608c