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2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE

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2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE Basic information

Product Name:
2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE
Synonyms:
  • 2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE
  • 2-(triphenylphosphoranylidene)propionaldehyde, 98 %
  • 2-(triphenylphosphoranylidene)
  • 2-(TRIPHENYLPHOSPHOR
  • 1-Formylethylidenetriphenylphosphorane
  • 2-(Triphenylphosphoranylidene)propanal
  • 2-(triphenyl-l5-phosphanylidene)propanal
  • 2-(Triphenylphosphoranylidene)propionaldehyde 98%
CAS:
24720-64-7
MF:
C21H19OP
MW:
318.35
Product Categories:
  • Aldehydes
  • Building Blocks
  • C13-C60
  • Carbonyl Compounds
  • C-C Bond Formation
  • Chemical Synthesis
  • C-C Bond Formation
  • Olefination
  • Wittig Reagents
  • Organic Building Blocks
  • Synthetic Reagents
  • Wittig Reagents
Mol File:
24720-64-7.mol
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2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE Chemical Properties

Melting point:
219-221 °C (lit.)
Boiling point:
478.5±28.0 °C(Predicted)
Density 
1.14±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
form 
Low Melting Solid
color 
White to pink to brown
CAS DataBase Reference
24720-64-7
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Safety Information

Risk Statements 
22-36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HS Code 
29319090

MSDS

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2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE Usage And Synthesis

Chemical Properties

White to light beige crystalline powder

Uses

Reactant for:• ;Preparation of acitretin analogs with antitumor activity1• ;Stereoselective synthesis of essential building blocks of phorboxazole A via hetero Diels-Alder and stereoselective hetero-Michael addition/equilibration2• ;Preparation of C1-C14 fragment of sarcoglaucol-16-one via Z-selective ando-type Horner-Wadsworth-Emmons olefination3• ;Wittig reactions4• ;Synthesis of ring-expanded and epothilone-hybridized macrosphelide analogs as apoptosis-inducing agents5• ;Preparation of phosphonic acid-containing analogs of mycophenolic acid as inhibitors

Uses

2-(Triphenylphosphoranylidene)propionaldehyde is a reagent used in the asymmetric synthesis of hispidanin A via oxidative alkoxylation and stereoselective Diels-Alder reaction. Also acts as a reagent in the stereoselective synthesis of 10-epi-tirandamycin E.

Uses

Reactant for:

  • Preparation of acitretin analogs with antitumor activity
  • Stereoselective synthesis of essential building blocks of phorboxazole A via hetero Diels-Alder and stereoselective hetero-Michael addition/equilibration
  • Preparation of C1-C14 fragment of sarcoglaucol-16-one via Z-selective ando-type Horner-Wadsworth-Emmons olefination
  • Wittig reactions
  • Synthesis of ring-expanded and epothilone-hybridized macrosphelide analogs as apoptosis-inducing agents
  • Preparation of phosphonic acid-containing analogs of mycophenolic acid as inhibitors of IMPDH

2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDESupplier

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