2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE
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
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
Safety Information
- Risk Statements
- 22-36/37/38
- Safety Statements
- 26-37/39
- WGK Germany
- 3
- HS Code
- 29319090
MSDS
- Language:English Provider:SigmaAldrich
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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2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE(24720-64-7)Related Product Information
- Ethyl 2-(triphenylphosphoranylidene)propionate
- 2-(TRIPHENYLPHOSPHORANYLIDENE)SUCCINIC ANHYDRIDE
- 2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE
- 2-(TRIPHENYLPHOSPHORANYLIDENE)BUTYRALDEHYDE
- 1-METHOXYCARBONYLETHYLIDENETRIPHENYLPHOSPHORANE
- ETHYL 4,4,4-TRIFLUORO-2-(TRIPHENYLPHOSPHORANYLIDENE)ACETOACETATE
- METHYL 2-[5-(4-CHLOROPHENYL)-2-HYDROXY-3-OXO-2,3-DIHYDROFURAN-2-YL]-2-(1,1,1-TRIPHENYL-LAMBDA5-PHOSPHANYLIDENE)ACETATE
- 2-[2-(4-CHLOROPHENYL)-2-OXO-1-(1,1,1-TRIPHENYL-LAMBDA5-PHOSPHANYLIDENE)ETHYL]-2-HYDROXY-5-PHENYL-2,3-DIHYDROFURAN-3-ONE
- ETHYL 2,4-DIOXO-3-(1,1,1-TRIPHENYL-LAMBDA5-PHOSPHANYLIDENE)PENTANOATE
- SPECS AE-848/33625045
- METHYL 2-(2-HYDROXY-3-OXO-5-PHENYL-2,3-DIHYDROFURAN-2-YL)-2-(1,1,1-TRIPHENYL-LAMBDA5-PHOSPHANYLIDENE)ACETATE
- METHYL 3-OXO-3-[3-(TRIFLUOROMETHYL)PHENYL]-2-(TRIPHENYLPHOSPHORANYLIDENE)PROPANOATE
- AURORA KA-1174
- AURORA KA-1073
- SALOR-INT L150010-1EA
- SALOR-INT L151815-1EA
- 4-[(4-BROMOPHENYL)(DIPHENYL)PHOSPHORANYLIDENE]-5-METHYL-2-PHENYL-2,4-DIHYDRO-3H-PYRAZOL-3-ONE
- AURORA KA-1180