Tricyclohexylphosphine
Suppliers
Names
[ CAS No. ]:
2622-14-2
[ Name ]:
Tricyclohexylphosphine
[Synonym ]:
Phosphine, tricyclohexyl-
triscyclohexylphosphine
Tricyclohexyl-phosphane
Tricyclohexylphosphine solution
EINECS 220-069-2
Tricyclohexylphosphine
PCy3
Phosphine,tricyclohexyl
tricyclohexylphosphan
MFCD00003853
bistricyclohexylphosphine
Tricyclohexyl Phosphine
Chemical & Physical Properties
[ Density]:
0.909 g/mL at 25 °C
[ Boiling Point ]:
383.4±9.0 °C at 760 mmHg
[ Melting Point ]:
81-83 °C(lit.)
[ Molecular Formula ]:
C18H33P
[ Molecular Weight ]:
280.428
[ Flash Point ]:
195.6±25.0 °C
[ Exact Mass ]:
280.231995
[ PSA ]:
13.59000
[ LogP ]:
7.00
[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C
[ Storage condition ]:
−20°C
MSDS
Safety Information
[ Symbol ]:
GHS02, GHS07, GHS08
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H225-H304-H315-H319-H335-H336-H361d-H373
[ Precautionary Statements ]:
P210-P261-P281-P301 + P310-P305 + P351 + P338-P331
[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
Xn:Harmful;
[ Risk Phrases ]:
R22;R36/37/38
[ Safety Phrases ]:
S26-S36/37-S62-S37/39-S36-S33-S29-S16
[ RIDADR ]:
UN 2056 3/PG 2
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
3.0
[ 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
Macromol. Rapid Commun. 36 , 1605-11, (2015)
Metal-organic frameworks (MOFs) nanoparticles in combination with a nonionic surfactant (Pluronic L-121) are used to stabilize dicyclopentadiene (DCPD)-in-water high internal phase emulsions (HIPEs). ...
Dalton Trans. 43(42) , 15997-6005, (2014)
Ni(0)-catalyzed dehydrogenation of benzylic-type imines was performed to yield asymmetrical tetra-substituted imidazoles and 2-imidazolines. This was achieved with a single operational step while main...
J. Am. Chem. Soc. 128(6) , 5350-5351, (2006)
Cyclopropyl phenyl ketone underwent oxidative addition to Ni(PCy3) generated from Ni(cod)2 and PCy3 to give a nickeladihydropyran, which is a key intermediate for the Ni(0)-catalyzed homo- or heterocy...