Dicyclohexylphenylphosphine

Product Information

Molecular Formula:
C18H27P
Molecular Weight:
274.38
Description
Dicyclohexylphenylphosphine is an indispensable reagent within the captivating realm of biomedicine. Its paramount significance unravels in its unrivaled contribution to the intricate synthesis of pharmaceutical drugs, harmonizing harmoniously with the multifaceted quest for revolutionary therapeutic agents tailored to assuage a myriad of enigmatic diseases.
Synonyms
dicyclohexylphenyl-phosphin; phenyldicyclohexylphosphine; Phosphine, dicyclohexylphenyl-; DICYCLOHEXYLPHENYLPHOSPHINE; PHENYLPHOSPHINODICYCLOHEXANE; dicyclohexylphenylphosphine95+%; Dicyclohexyphenylphosphine; PHENYLDICYCLOHEXYLPHOSPHINE(PHPCY2)
IUPAC Name
dicyclohexyl(phenyl)phosphane
Canonical SMILES
C1CCC(CC1)P(C2CCCCC2)C3=CC=CC=C3
InChI
InChI=1S/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
InChI Key
VPLLTGLLUHLIHA-UHFFFAOYSA-N
Melting Point
60-61 °C (lit.)
Flash Point
Not applicable
Purity
>95.0%(GC)
Appearance
White to off-white crystalline powder

Safety Information

Hazards
H302

Computed Properties

XLogP3
5.1
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
3
Exact Mass
274.185037859 g/mol
Monoisotopic Mass
274.185037859 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
19
Formal Charge
0
Complexity
226
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113831272-A Method for synthesizing 2-substituted indole compound by using palladium to catalyze iodobenzene and oxime ester 2021-09-26
CN-113105374-A Method for synthesizing alkylamine derivative 2021-04-14
CN-113149971-A 8- (indoletriazole) substituted coumarin compound and preparation method and application thereof 2021-03-05
CN-112552215-A Method for synthesizing allyl amine derivative 2020-12-10
CN-114181250-A Alkenyl phosphine compound and preparation method thereof 2020-09-15
KR-20220022349-A (ALKYL)ARENES AND A Method for Producing the Same 2020-08-18
WO-2022006427-A1 Manufacturing process for 3,5-dichloropicolinonitrile for synthesis of vadadustat 2020-07-02
WO-2022003040-A1 Process for treating keratin fibers using particular amino acids in high concentration 2020-06-30
JP-2022022505-A Method for producing alkynylsilane 2020-06-24
CN-113801111-A Biphenyl derivative inhibitor and preparation method and application thereof 2020-06-12

Literatures

PMID Publication Date Title Journal
22580400 2012-05-11 Development of a method for the preparation of ruthenium indenylidene-ether olefin metathesis catalysts Molecules (Basel, Switzerland)
22589787 2012-04-01 trans-Dichloridobis[dicyclo-hex-yl(phen-yl)phosphane-κP]palladium(II) Acta crystallographica. Section E, Structure reports online
21775812 2011-08-01 Deducing chemical structure from crystallographically determined atomic coordinates Acta crystallographica. Section B, Structural science
21753995 2011-04-01 Bis[dicyclo-hexyl-(phenyl)-phosphane-κP]silver(I) perchlorate dichloro-methane monosolvate Acta crystallographica. Section E, Structure reports online
21579003 2010-04-10 Bis(dicyclo-hexyl-phenyl-phosphine)silver(I) nitrate Acta crystallographica. Section E, Structure reports online
21578100 2009-10-10 Bis(dicyclo-hexyl-phenyl-phosphine)iodido-silver(I) pyridine monosolvate Acta crystallographica. Section E, Structure reports online
21582395 2009-03-30 Di-μ-iodido-bis-{[dicyclo-hexyl(phen-yl)phosphine-κP](pyridine-κN)silver(I)} Acta crystallographica. Section E, Structure reports online
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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