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
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 |
