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Lawesson reagent

ALDRICH/227439 - 97%

Synonym: 2,4-Bis(4-methoxyphenyl)-2,4-dithioxo-1,3,2,4-dithiadiphosphetane; 2,4-Bis-(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide; 4-Methoxyphenylthiophosphoric cyclic di(thioanhydride); LR

CAS Number: 19172-47-5
Empirical Formula (Hill Notation): C14H14O2P2S4
Molecular Weight: 404.47
MDL Number: MFCD00005171
Linear Formula: C14H14O2P2S4
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-227439-10G 10 g
$46.80
1/EA
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45-227439-25G 25 g
$57.20
1/EA
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45-227439-100G 100 g
$120.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 227439-100G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 227439-10G

 

assay 97%
form powder
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
InChI key CFHGBZLNZZVTAY-UHFFFAOYSA-N
mp 228-230 °C (lit.)
Quality Level 100 
SMILES string COc1ccc(cc1)P2(=S)SP(=S)(S2)c3ccc(OC)cc3
Application: 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.
General description: 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.
Packaging: 10, 25, 100 g in glass bottle
Symbol GHS02  GHS02
Signal word Danger
Hazard statements H261
Precautionary statements P231 + P232 - P422
Hazard Codes F
Risk Statements 15/29
Safety Statements 7/8-43
RIDADR UN 3134 6.1(4.3) / PGII
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Supplemental Hazard Statements EUH029
Purity 97%
mp 228-230 °C (lit.)
UNSPSC 12352005

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