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Merck

227439

Sigma-Aldrich

Lawesson-Reagenz

97%

Synonym(e):

2,4-Bis-[4-methoxyphenyl]-1,3-dithia-2,4-diphosphetan-2,4-disulfid, 4-Methoxy-phenylthiophosphonsäure-cycl.-di-thioanhydrid, LR, Phosphorpentasulfid-Ersatz

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About This Item

Empirische Formel (Hill-System):
C14H14O2P2S4
CAS-Nummer:
Molekulargewicht:
404.47
Beilstein:
1024888
MDL-Nummer:
UNSPSC-Code:
12352005
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

Assay

97%

Form

powder

mp (Schmelzpunkt)

228-230 °C (lit.)

SMILES String

COc1ccc(cc1)P2(=S)SP(=S)(S2)c3ccc(OC)cc3

InChI

1S/C14H14O2P2S4/c1-15-11-3-7-13(8-4-11)17(19)21-18(20,22-17)14-9-5-12(16-2)6-10-14/h3-10H,1-2H3

InChIKey

CFHGBZLNZZVTAY-UHFFFAOYSA-N

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Allgemeine Beschreibung

Lawesson′s reagent is generally used as a thiation agent in organic synthesis for the conversion of oxygen functionalities into their thio analogs. It facilitates the conversion of the carbonyl group to thiocarbonyl group as well as carbon-oxygen single bond into a carbon-sulfur single bond.

Anwendung

Lawesson reagent can be used as a reagent to synthesize:
  • Oxthiaphosphinine-3-sulfide derivatives by the reaction with Mannich bases of β-naphthol and 8-hydroxyquinoline.
  • 1,3,5,2-Trithiaphosphinane-2-sulfide derivatives by reacting with benzaldehyde in the presence of trialkyl phosphite.
  • 2,4,6-Triphenyl-1,3,5-trithiane from benzaldehyde and ethyl acrylate.
  • 9-Benzanthronethione by thionation of 9-benzanthone oxime.
  • 1,2,4-Trithiolane from 2,2,4,4-tetramethyl-3-thioxocyclobutanone S-oxide.
  • Sulfur derivatives of triterpenic oxo compounds.
  • Tropothione in situ at room temperature and to trap it with dieneophiles.

Piktogramme

Flame

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Water-react 2

Zusätzliche Gefahrenhinweise

Lagerklassenschlüssel

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Reaction of lupane and oleanane triterpenoids with Lawesson's reagent
Kvasnica M, et al.
Tetrahedron, 64(17), 3736-3743 (2008)
T Nakai et al.
Solid state nuclear magnetic resonance, 4(3), 163-171 (1995-03-01)
The nuclear magnetic resonance (NMR) powder patterns observed for the 31P spin pair in Lawesson's reagent (1) were analyzed. Using an efficient procedure, wide ranges of the spin parameters were examined to determine whether they might reproduce the experimental one-dimensional
Frédéric Peyrane et al.
Chemical communications (Cambridge, England), (6)(6), 736-737 (2003-04-22)
Treatment of 2'-deoxy-3',5'-dithexyldimethylsilyl-5,6-dihydrouridine with Lawesson's reagent led to the expected C4-thiolated derivative together with a number of oxathiaphosphepane isomers which resulted from the heat reversible incorporation of an AnPS2 unit within the 2'-deoxyribose moiety explaining the subsequent anomerisation of the
The direct formation of glycosyl thiols from reducing sugars allows one-pot protein glycoconjugation.
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Angewandte Chemie (International ed. in English), 45(24), 4007-4011 (2006-05-05)
M de Neeling et al.
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