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Sigma-Aldrich

1-(Triphenylphosphoranylidene)-2-propanone

99%

Synonym(s):

(2-Oxopropylidene)triphenylphosphorane, Acetylmethylene-triphenylphosphorane, Methyl (triphenylphosphoranylidene)methyl ketone, NSC 407394

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About This Item

Linear Formula:
CH3COCH=P(C6H5)3
CAS Number:
Molecular Weight:
318.35
Beilstein:
750077
EC Number:
MDL number:
UNSPSC Code:
12352115
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

solid

reaction suitability

reaction type: C-C Bond Formation

mp

203-205 °C (lit.)

SMILES string

CC(=O)C=P(c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/C21H19OP/c1-18(22)17-23(19-11-5-2-6-12-19,20-13-7-3-8-14-20)21-15-9-4-10-16-21/h2-17H,1H3

InChI key

KAANTNXREIRLCT-UHFFFAOYSA-N

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Related Categories

Application

Reactant for:
  • Cascade reactions of enals for enantioselective synthesis of indane derivatives
  • Enantioselective conjugate addition for synthesis of α-branched indoles
  • Synthesis of 1,2-dioxanes with antitrypanosomal activity
  • Asymmetric allylboration for enantioselective synthesis of (+)-awajanomycin
  • Domino Suzuki / Heck coupling reactions for preparation of fluorenylidenes
  • Synthesis of amphibian pyrrolizidine alkaloids via allylic aminations
  • Synthesis of silicon-containing acyclic dienone musk odorants
Wittig reagent used recently in the syntheses of functionalized pyrrolidines and cyclobutanones.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis, 1359-1359 (2007)
Martin A Lovchik et al.
The Journal of organic chemistry, 72(7), 2427-2433 (2007-03-06)
Mechanistic studies on the intramolecular nucleophilic substitution with allylic rearrangement (SNi' reaction) and a new stereoselective access to substituted cyclobutanones are reported. 4,4-Dialkyl-5-oxohex-2E-en-1-yl methanesulfonates 4 were converted to 2,2-dialkyl-3-vinylcyclobutanones 6 by SNi' ring closure. The stereochemical analysis of the reaction
Liang-Chieh Chen et al.
Frontiers in pharmacology, 9, 708-708 (2018-07-19)
Alzheimer's disease (AD) is a progressive neurodegenerative disorder with multiple etiologies. Beta-amyloid (Aβ) self-aggregation and overexpression of class IIa histone deacetylases (HDACs) are strongly implicated with AD pathogenesis. In this study, a series of novel diarylheptanoid derivatives were designed, synthesized

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