ISOPROPYLDIPHENYLPHOSPHINE
Product Information
Molecular Formula
C15H17P
Molecular Weight
228.27
Description
Catalyst in:• Nickel/Lewis acid-catalyzed aryl- and alkenylcyanation of unsaturated bonds• Nickel/Lewis Acid-Catalyzed Cyanoesterification and Cyanocarbamoylation of Alkynes• Methoxycarbonylation reactions (palladium complex)• Decarboxylative cross-coupling in the presence of palladium• Asymmetric hydrogenation of quinolines catalyzed by iridium complexes of BINOL-derived diphosphonites• Hydroesterification of vinylarenes in complex with palladium• Ligand precatalyst for room-temperature Heck coupling reactions
Synonyms
ISOPROPYLDIPHENYLPHOSPHINE; DIPHENYL-ISO-PROPYLPHOSPHINE; i-Propyldiphenylphosphine,99%; I-PROPYLDIPHENYLPHOSPHINE; Einecs 228-902-1; Phosphine, (1-methylethyl)diphenyl-
IUPAC Name
diphenyl(propan-2-yl)phosphane
SMILES
CC(C)P(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChI=1S/C15H17P/c1-13(2)16(14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-13H,1-2H3
InChI Key
LLZAIAIZAVMQIG-UHFFFAOYSA-N
Boiling Point
165 °C/11 mmHg (lit.)
Melting Point
40-43 °C (lit.)
Flash Point
235.4 °F - closed cup
Purity
>97.0%(GC)
Density
0.861
Safety Information
Hazards
H315 - H319 - H335
Precautionary Statement
P302 + P352 - P305 + P351 + P338
Computed Properties
XLogP3
3.9
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
3
Exact Mass
228.106787540 g/mol
Monoisotopic Mass
228.106787540 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
170
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 |
|---|---|---|
| KR-20220022349-A | (ALKYL)ARENES AND A Method for Producing the Same | 2020-08-18 |
| WO-2021230194-A1 | Composition | 2020-05-14 |
| WO-2021230195-A1 | Composition | 2020-05-14 |
| CN-111518145-A | Cyanide-bridged metal organic compound with intramolecular magnetic transformation, and preparation method and application thereof | 2020-05-07 |
| WO-2021219418-A1 | Preparation of aromatic carboxyamides by palladium-catalyzed carbonylation reaction | 2020-04-29 |
| WO-2021219424-A1 | Preparation of aromatic carboxyamides by a palladium-catalyzed carbonylation reaction | 2020-04-29 |
| JP-2021161333-A | Polycarbonate resin composition and its molded product | 2020-04-02 |
| DE-202020001249-U1 | Hydroxyalkyl acrylate based monomers for use as reactive diluents in printing formulations | 2020-04-01 |
| JP-2021138910-A | Modified epoxidized polybutadiene, epoxy resin composition and cured product and can paint and can coating | 2020-03-06 |
| KR-20210101082-A | (arylmethyl)arenes and a production process thereof | 2020-02-07 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 5789 | 1976-04-01 | Hyperoxia and red cell 2,3-diphosphoglycerate | Toxicology and applied pharmacology |
