Tricyclohexylphosphine structure
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Common Name | Tricyclohexylphosphine | ||
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CAS Number | 2622-14-2 | Molecular Weight | 280.428 | |
Density | 0.909 g/mL at 25 °C | Boiling Point | 383.4±9.0 °C at 760 mmHg | |
Molecular Formula | C18H33P | Melting Point | 81-83 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 195.6±25.0 °C | |
Symbol |
GHS02, GHS07, GHS08 |
Signal Word | Danger |
Name | tricyclohexylphosphane |
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Synonym | More Synonyms |
Density | 0.909 g/mL at 25 °C |
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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 |
Symbol |
GHS02, GHS07, GHS08 |
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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 |
Precursor 10 | |
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DownStream 9 | |
HS Code | 2931900090 |
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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% |
Synthesis and Catalytic Performance of Hierarchically Porous MIL-100(Fe)@polyHIPE Hybrid Membranes.
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). ... |
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Synthesis of tetra-substituted imidazoles and 2-imidazolines by Ni(0)-catalyzed dehydrogenation of benzylic-type imines.
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... |
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Formation of nickeladihydropyran by oxidative addition of cyclopropyl ketone. Key intermediate in nickel-catalyzed cycloaddition.
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... |
Phosphine, tricyclohexyl- |
triscyclohexylphosphine |
Tricyclohexyl-phosphane |
Tricyclohexylphosphine solution |
EINECS 220-069-2 |
Tricyclohexylphosphine |
PCy3 |
Phosphine,tricyclohexyl |
tricyclohexylphosphan |
MFCD00003853 |
bistricyclohexylphosphine |
Tricyclohexyl Phosphine |