6476-37-5 Usage
Description
Dicyclohexylphenylphosphine is an organic phosphine compound characterized by its unique structure that features a phosphorus atom bonded to a phenyl group and two cyclohexyl rings. Dicyclohexylphenylphosphine is known for its versatile chemical properties and reactivity, making it a valuable component in various chemical processes and reactions.
Uses
Used in Organic Synthesis:
Dicyclohexylphenylphosphine is used as a raw material for organic synthesis due to its ability to participate in a wide range of chemical reactions. Its phosphorus center can act as a nucleophile, facilitating the formation of new chemical bonds and aiding in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Dicyclohexylphenylphosphine is utilized as a reagent or intermediate in the production of various pharmaceutical compounds. Its unique properties allow it to be involved in the synthesis of drugs with specific therapeutic effects, contributing to the development of new medications.
Used in Chemical Research:
Dicyclohexylphenylphosphine is also employed in chemical research as a model compound for studying the reactivity and behavior of phosphorus-containing compounds. Researchers use this compound to gain insights into the mechanisms of various chemical reactions and to develop new synthetic methodologies.
Used in Material Science:
In the field of material science, Dicyclohexylphenylphosphine can be used as a precursor for the development of new materials with specific properties. Its ability to form stable complexes and participate in coordination chemistry makes it a promising candidate for the creation of advanced materials with applications in various industries.
Overall, Dicyclohexylphenylphosphine is a versatile organic phosphine compound with a wide range of applications in organic synthesis, pharmaceuticals, chemical research, and material science. Its unique structure and reactivity make it an essential component in the development of new chemical processes and products.
Check Digit Verification of cas no
The CAS Registry Mumber 6476-37-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6476-37:
(6*6)+(5*4)+(4*7)+(3*6)+(2*3)+(1*7)=115
115 % 10 = 5
So 6476-37-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H27P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1,4-5,10-11,17-18H,2-3,6-9,12-15H2
6476-37-5Relevant articles and documents
31P Nuclear Magnetic Resonance Studies of Polymer-Anchored Rhodium(I) Complexes
Naaktgeboren, Aart J.,Nolte, Roeland J. M.,Drenth, Wiendelt
, p. 3350 - 3354 (1980)
Poly(4-diphenylphosphinostyrene) (1), poly(4-dicyclohexylphosphinostyrene) (2), and poly (3) were obtained by polymerization of the corresponding monomers.The polymers were treated with (RhClL2)2 and with (RhClL')2, where L and L' are ethene and 1,5-cyclooctadiene, respectively.These complexes were added stepwise and during this process the 31P NMR spectra were observed. 31P chemical shifts and 103Rh-31P coupling constants were compared with those of monomeric analogues which were treated in the same way.
Palladium-Catalyzed C-P(III) Bond Formation by Coupling ArBr/ArOTf with Acylphosphines
Chen, Xingyu,Wu, Hongyu,Yu, Rongrong,Zhu, Hong,Wang, Zhiqian
, p. 8987 - 8996 (2021/06/30)
Palladium-catalyzed C-P bond formation reaction of ArBr/ArOTf using acylphosphines as differential phosphination reagents is reported. The acylphosphines show practicable reactivity with ArBr and ArOTf as the phosphination reagents, though they are inert to the air and moisture. The reaction affords trivalent phosphines directly in good yields with a broad substrate scope and functional group tolerance. This reaction discloses the acylphosphines' capability as new phosphorus sources for the direct synthesis of trivalent phosphines.
Preparation of Aryl(dicyclohexyl)phosphines by C-P Bond-Forming Cross-Coupling in Water Catalyzed by an Amphiphilic-Resin-Supported Palladium Complex
Hirai, Yoshinori,Uozumi, Yasuhiro
supporting information, p. 2966 - 2970 (2017/10/26)
Aryl(dicyclohexyl)phosphines were prepared by a catalytic C-P bond-forming cross-coupling reaction of haloarenes with dicyclohexylphosphine under heterogeneous conditions in water containing an immobilized palladium complex coordinated to an amphiphilic polystyrene-poly(ethylene glycol) resin supported di(tert -butyl)phosphine ligand.
