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Identification
CAS Number
37943-90-1
Name
Diphenyl-2-pyridylphosphine
Synonyms
2-(Diphenylphosphino)pyridin 2-(Diphenylphosphino)pyridine 2-(Diphénylphosphino)pyridine 2-diphenylphosphanyl-pyridine2-diphenylphosphinopyridine2-pyridyldiphenylphosphine37943-90-1 diphenyl(2-pyridinyl)phosphineDiphenyl-2-pyridylphosphine MFCD00192108 Pyridine, 2-(diphenylphosphino)- 2-(diphenylphosphanyl)pyridine2-(Diphenylphosphino)pyridine|2-(Diphenylphosphanyl)pyridine98%bisphenyl-(pyridin-2-yl)phosphineDiphenyl 2-pyridyl phosphinediphenyl(2-pyridyl)phosphinediphenyl(pyridin-2-yl)phosphanediphenylphosphino-pyridinediphenylpyridinylphosphineDPPPYOR-0960
SMILES
c1ccc(cc1)P(c2ccccc2)c3ccccn3
StdInChI
InChI=1S/C17H14NP/c1-3-9-15(10-4-1)19(16-11-5-2-6-12-16)17-13-7-8-14-18-17/h1-14H
StdInChIKey
SVABQOITNJTVNJ-UHFFFAOYSA-N
Molecular Formula
C17H14NP
Molecular Weight
263.273
MDL Number
MFCD00192108
Properties
Appearance
White to Off-white crystalline powder
Safety Data
Symbol
GHS07
Signal Word
Warning
Hazard statements
H315,H319,H335,H413
Precautionary Statements
P261 - P264 - P271 - P273 - P302 + P352 - P305 + P351 + P338
WGK Germany
3
MSDS Download
Specifications and Other Information of Our Diphenyl-2-pyridylphosphine CAS 37943-90-1
Identification Methods
HNMR, HPLC
Purity
99% min
Melting Point
82~83℃
Shelf Life
1 year
Storage
Slowly oxidized in the air for a long time, vacuum pack, and store in cold storage
Known Application
Ligand in metal-catalyzed reactions:
Carbonylation: Facilitates the introduction of carbonyl groups into organic molecules.Hydration: Aids in the addition of water to unsaturated compounds, forming alcohols or other functionalized derivatives.Dehydrogenative coupling: Promotes coupling reactions by removing hydrogen, often forming C-C or C-N bonds.Carbostannylation: Catalyzes the introduction of stannyl (Sn) groups into organic compounds.Dimethylstannylation: Specific variant of stannylation, introducing dimethylstannyl groups.Silylation: Facilitates the introduction of silyl groups, improving stability and reactivity of substrates.Reagent in Mitsunobu reactions:
Used in the conversion of alcohols to various functional groups, such as esters, ethers, or amines, under mild conditions.
General View of Documents
Links
This product is developed by our R&D company Warshel Chemical Ltd (https://www.warshel.com/).
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