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Dicyclohexylphosphine
[CAS# 829-84-5]

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Complete supplier list of Dicyclohexylphosphine
Identification
Classification Organic raw materials >> Organic phosphine compound
Name Dicyclohexylphosphine
Molecular Structure CAS # 829-84-5, Dicyclohexylphosphine
Molecular Formula C12H23P
Molecular Weight 198.28
CAS Registry Number 829-84-5
EC Number 212-590-9
SMILES C1CCC(CC1)PC2CCCCC2
Properties
Melting point 129 ºC (8mmHg)
Refractive index 1.516
Safety Data
Hazard Symbols symbol symbol symbol symbol symbol   GHS02;GHS05;GHS06;GHS07;GHS09 Danger    Details
Hazard Statements H225-H250-H301+H311+H331-H301-H311-H314-H319-H331-H411    Details
Precautionary Statements P210-P222-P231-P233-P240-P241-P242-P243-P260-P261-P262-P264-P264+P265-P270-P271-P273-P280-P301+P316-P301+P330+P331-P302+P335+P334-P302+P352-P302+P361+P354-P303+P361+P353-P304+P340-P305+P351+P338-P305+P354+P338-P316-P321-P330-P337+P317-P361+P364-P363-P370+P378-P391-P403+P233-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Pyrophoric liquidsPyr. Liq.1H250
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.3H301
Acute toxicityAcute Tox.3H311
Acute toxicityAcute Tox.3H331
Flammable liquidsFlam. Liq.2H225
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Skin corrosionSkin Corr.1AH314
Specific target organ toxicity - single exposureSTOT SE3H335
Flammable liquidsFlam. Liq.1H224
Acute toxicityAcute Tox.4H302
Skin irritationSkin Irrit.2H315
SDS Available
up Discovory and Applicatios
Dicyclohexylphosphine is a notable organophosphorus compound with significant applications in chemistry, particularly in catalysis and organic synthesis. This chemical substance is characterized by the presence of two cyclohexyl groups attached to a central phosphorus atom, forming a stable phosphine ligand. The synthesis of dicyclohexylphosphine involves the reaction of cyclohexylmagnesium bromide with a phosphorus trichloride precursor, resulting in the formation of the desired phosphine.

The discovery of dicyclohexylphosphine can be traced back to efforts aimed at developing new ligands for transition metal complexes. Its structure, which incorporates bulky cyclohexyl groups, imparts steric hindrance around the phosphorus atom. This steric bulk is crucial in stabilizing metal complexes and influencing their reactivity. The presence of these bulky groups helps to reduce the likelihood of ligand dissociation, thereby enhancing the stability of the metal center.

In terms of applications, dicyclohexylphosphine is widely used as a ligand in various catalytic processes. Its effectiveness as a ligand is particularly evident in transition metal catalysis, where it plays a crucial role in facilitating reactions such as hydrogenation, cross-coupling, and hydroformylation. The bulky cyclohexyl groups provide significant steric protection, making the ligand highly effective in stabilizing metal centers and promoting specific catalytic transformations.

Additionally, dicyclohexylphosphine is employed in the synthesis of complex organic molecules. It is used to form organometallic compounds that serve as intermediates in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The ligand's ability to coordinate with various metals allows for the formation of a range of metal complexes, each with tailored reactivity suitable for different synthetic applications.

The compound also finds use in material science, particularly in the development of advanced materials with specific properties. The phosphine's role in stabilizing metal centers can be exploited to create materials with desirable mechanical, electrical, or catalytic properties.

Overall, dicyclohexylphosphine represents an important advancement in the field of organophosphorus chemistry. Its discovery and applications highlight the significance of phosphine ligands in enhancing the stability and reactivity of metal complexes, making it a valuable tool in both industrial and academic research.
Market Analysis Reports
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