Thiirane, phenyl-, (R)-

Base Information

Chemical Name:Thiirane, phenyl-, (R)-
CAS No.:33877-15-5
Molecular Formula:C8H8S
Molecular Weight:136.218
Hs Code.:
DSSTox Substance ID:DTXSID30481328
Nikkaji Number:J1.123.438K
Wikidata:Q82316670

Synonyms:Thiirane, phenyl-, (R)-;33877-15-5;DTXSID30481328

Suppliers and Price of Thiirane, phenyl-, (R)-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Thiirane, phenyl-, (R)-

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:136.03467143
Heavy Atom Count:9
Complexity:94.7

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(S1)C2=CC=CC=C2
Isomeric SMILES:C1[C@H](S1)C2=CC=CC=C2

Technology Process of Thiirane, phenyl-, (R)-

There total 4 articles about Thiirane, phenyl-, (R)- 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: 90.0%

: 20780-53-4
(R)-Styrene oxide

: 33877-15-5
(R)-(+)-styrene sulfide

: (S)-(+)-styrene episulfide

Guidance literature:: With ammonium thiocyanate; cerium(IV) trifluoromethanesulfonate; In acetonitrile; at -10 ℃; for 2h; Title compound not separated from byproducts;
DOI:10.1080/00397919908085959

Reference yield: 77.0%

: 141561-41-3,141561-42-4,141561-45-7,141561-46-8
<(SR)-2-Chloro-2-phenylethyl>-2,3:5,6-di-O-isopropyliden-β-D-mannofuran

: 33877-15-5
(R)-(+)-styrene sulfide

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at -30 - -20 ℃; for 16h;
DOI:10.1002/hlca.19920750215

Reference yield: 40.0%

: 96-09-3
styrene oxide

: 20780-53-4
(R)-Styrene oxide

: 33877-15-5
(R)-(+)-styrene sulfide

Guidance literature:: With (R)-3,3'-bis(2,4,6-triisopropylphenyl)binol phosphoric acid; 3,4-dihydro-(1H)-quinoline-2-thione; In chloroform; at -20 - 20 ℃; for 53h; Reagent/catalyst; Time; enantioselective reaction; Mechanism;
DOI:10.1021/jacs.6b01960