(Triphenylphosphoranylidene)acetaldehyde
Suppliers
Names
[ CAS No. ]:
2136-75-6
[ Name ]:
(Triphenylphosphoranylidene)acetaldehyde
[Synonym ]:
Ph3P=CH-CHO
Trippett's reagent
(Formylmethylene)triphenylphosphorane
(Triphenylphosphoranylidene)acetaldehyde
2-[Methylene(diphenyl)phosphoranyl]benzaldehyde
triphenylphosphoranylideneacetaldehyde
Benzaldehyde, 2-(methylenediphenylphosphoranyl)-
EINECS 218-375-6
MFCD00006994
Chemical & Physical Properties
[ Density]:
1.2±0.1 g/cm3
[ Boiling Point ]:
486.9±47.0 °C at 760 mmHg
[ Melting Point ]:
185-188 °C(lit.)
[ Molecular Formula ]:
C20H17OP
[ Molecular Weight ]:
304.32
[ Flash Point ]:
248.3±29.3 °C
[ Exact Mass ]:
304.101715
[ PSA ]:
26.88000
[ LogP ]:
3.80
[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C
[ Index of Refraction ]:
1.615
[ Storage condition ]:
Keep Cold
[ Stability ]:
Stable. Combustible. Incompatible with strong oxidizing agents.
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2931900090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2931900090
[ Summary ]:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%
Articles
J. Org. Chem. 72 , 2744, (2007)
The total synthesis of borrelidin has been achieved. The best feature of our synthetic route is macrocyclization at C11-C12 for the construction of an 18-membered ring after esterification between two...
Org. Lett. 9 , 3703, (2007)
The first total synthesis of (-)-aplysiallene has been completed in 16 steps and features a key sequential Mukaiyama aerobic oxidative cyclization to prepare the fused bis-THF core. The original stere...
H.J. Bestmann et al.Angew. Chem. Int. Ed. Engl. 91 , 748, (1979)