| Identification | More | [Name]
Cyclohexyldiphenylphosphine | [CAS]
6372-42-5 | [Synonyms]
CYCLOHEXYLDIPHENYLPHOSPHINE
DIPHENYLCYCLOHEXYLPHOSPHINE
DIPHENYLPHOSPHINOCYCLOHEXANE
cyclohexyldiphenyl-phosphin
whitextl
Cyclohexyldiphenylphosphine,98%
DIPHENYLCYCLOHEXYLPHOSPHINE(PH2PCY)
CYCLOHEXYLDIPHENYLPHOSPHINE (DPCP)
Cyclohexyl-di(phenyl)phosphane | [EINECS(EC#)]
228-904-2 | [Molecular Formula]
C18H21P | [MDL Number]
MFCD00046360 | [Molecular Weight]
268.33 | [MOL File]
6372-42-5.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powde | [Melting point ]
58-62 °C(lit.)
| [Boiling point ]
374.0±11.0 °C(Predicted) | [Fp ]
>230 °F
| [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
Powder | [color ]
White | [Water Solubility ]
insoluble | [Sensitive ]
Air Sensitive | [InChI]
InChI=1S/C18H21P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-2,4-7,10-13,18H,3,8-9,14-15H2 | [InChIKey]
ZXKWUYWWVSKKQZ-UHFFFAOYSA-N | [SMILES]
P(C1CCCCC1)(C1=CC=CC=C1)C1=CC=CC=C1 | [CAS DataBase Reference]
6372-42-5(CAS DataBase Reference) | [EPA Substance Registry System]
Phosphine, cyclohexyldiphenyl- (6372-42-5) |
| Safety Data | Back Directory | [Risk Statements ]
36/37/38 | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
SY8387500
| [TSCA ]
No | [HS Code ]
29319090 |
| Hazard Information | Back Directory | [Description]
Cyclohexyldiphenylphosphine is a chemical compound commonly used as a ligand in coordination chemistry and organometallic synthesis. It acts as a stabilizing agent and facilitates various catalytic reactions. This compound finds applications in pharmaceuticals, fine chemicals, and materials science industries. Cyclohexyldiphenylphosphine should be handled with caution as it may cause skin and eye irritation. It should be stored in a cool, well-ventilated area away from heat sources or open flames. Proper personal protective equipment (PPE) should be worn when handling this compound. Not for human consumption. Such as Silver(I) phosphine complexes were synthesized by a reaction of AgNO3, AgCl, and AgBr with cyclohexyl diphenylphosphine to produce 1:1, 1:2, or 1:3 molar ratios of new silver complexes[1].
| [Chemical Properties]
white to light yellow crystal powde | [Uses]
suzuki reaction | [References]
[1] Naganagowda, Gadada et al. “Synthesis, crystal structure and spectral studies of silver(I) cyclohexyldiphenylphosphine complexes: towards the biological evaluation on malignant and non-malignant cells.” Journal of Coordination Chemistry 21 1 (2023): 0. |
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