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Diphenyl-2-pyridylphosphine

CAS No.
37943-90-1
Chemical Name:
Diphenyl-2-pyridylphosphine
Synonyms
2-(DIPHENYLPHOSPHINO)PYRIDINE;2-Pyridyldiphenylphosphine;2-(diphenylphosphanyl)pyridine;-2-pyridyL;DPPPY/DIPHENYL-2-PYRIDYL;DIPHENYL-2-PYRIDYLPHOSPHINE;Diphenyl(2-pyridyl)phosphane;Diphenyl(2-pyridinyl)phosphine;Diphenyl-2-pyridylphosphine>Diphenyl-2-pyridylphosphine 97%
CBNumber:
CB0763330
Molecular Formula:
C17H14NP
Molecular Weight:
263.27
MDL Number:
MFCD00192108
MOL File:
37943-90-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 22:55:03

Diphenyl-2-pyridylphosphine Properties

Melting point 82-84 °C (dec.) (lit.)
Boiling point 163 °C(Press: 0.05 Torr)
storage temp. Inert atmosphere,Room Temperature
solubility Soluble in toluene. (almost transparency)
pka 2.37±0.12(Predicted)
form Crystalline Powder
color White to yellow to tan
InChI 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
InChIKey SVABQOITNJTVNJ-UHFFFAOYSA-N
SMILES C1(P(C2=CC=CC=C2)C2=CC=CC=C2)=NC=CC=C1
CAS DataBase Reference 37943-90-1(CAS DataBase Reference)
FDA UNII 4K685YSU7Y
UNSPSC Code 12352005
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335-H413
Precautionary statements  P273-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  29333990
Storage Class 11 - Combustible Solids
Hazard Classifications Aquatic Chronic 4
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

Diphenyl-2-pyridylphosphine price More Price(94)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 392960 Diphenyl-2-pyridylphosphine 97% 37943-90-1 5g $116 2026-04-30 Buy
TCI Chemical D2471 Diphenyl-2-pyridylphosphine >97.0%(GC) 37943-90-1 1g $19 2026-04-30 Buy
TCI Chemical D2471 Diphenyl-2-pyridylphosphine >97.0%(GC) 37943-90-1 5g $37 2026-04-30 Buy
Strem Chemicals 15-1780 2-Diphenylphosphinopyridine, min. 97% 37943-90-1 5g $78 2026-04-30 Buy
Strem Chemicals 15-1780 2-Diphenylphosphinopyridine, min. 97% 37943-90-1 25g $309 2026-04-30 Buy
Product number Packaging Price Buy
392960 5g $116 Buy
D2471 1g $19 Buy
D2471 5g $37 Buy
15-1780 5g $78 Buy
15-1780 25g $309 Buy

Diphenyl-2-pyridylphosphine Chemical Properties,Uses,Production

Reaction

Ligand for the palladium-catalyzed distannylation of ortho-quinodimethanes
Ligand for the palladium-catalyzed disilylation of o-quinodimethanes to synthesize 9- and 10-membered disilacarbocycles
Ligand for the palladium-catalyzed alkoxycarbonylation of allenes Reactions of 37943-90-1

Chemical Properties

Yellow to orange crystalline powder

Uses

Diphenyl-2-pyridylphosphine is an organophosphorous compound that is a widely used mono-pyridylphosphine ligand in transition metal complexes for catalysis.

Uses

suzuki reaction

Uses

Ligand for metal-catalyzed carbonylations, hydration, dehydrogenative coupling, carbostannylation, distannylation, and silylation; reagent for Mitsunobu reaction.

Application

Diphenyl-2-pyridylphosphine is a functionally diverse and important fine chemical. Its core value lies in its participation in catalytic reactions as an efficient ligand, thus playing a key role in drug synthesis, new materials development, and the chemical industry.

reaction suitability

reagent type: ligand
reaction type: Carbonatations
reagent type: ligand
reaction type: Dehydrogenation
reagent type: ligand
reaction type: Hydration Reaction
reagent type: ligand
reaction type: Mitsunobu Reaction
reagent type: ligand
reaction type: Stannylation

Synthesis

2-Iodopyridine

5029-67-4

Diphenylphosphine

829-85-6

Diphenyl-2-pyridylphosphine

37943-90-1

General procedure for the synthesis of diphenyl-2-pyridylphosphine from 2-iodopyridine and diphenylphosphine: MCM-41-3N-Pd(0) (21 mg, 0.01 mmol), KOAc (1.5 mmol), and 2-iodopyridine (1.0 mmol, if solid) were placed in an oven-dried 20 mL Schlenk tube. The vessel was evacuated and displaced three times with argon. Subsequently, 2-iodopyridine (1.0 mmol, if liquid), diphenylphosphine (1.2 mmol) and DMAc (1 mL) were added by syringe under argon protection. The reaction mixture was stirred at 130 °C for 3 hours. After the reaction was completed, the mixture was cooled to room temperature, diluted with CH2Cl2 (20 mL) and filtered.The MCM-41-3N-Pd(0) catalyst was washed with distilled water (2 × 5 mL) and ethanol (2 × 5 mL) for next use. The filtrate was concentrated under vacuum and the residue was purified by fast column chromatography on silica gel to obtain the target product diphenyl-2-pyridylphosphine.

References

[1] Journal of Organometallic Chemistry, 2018, vol. 866, p. 50 - 58
[2] Applied Organometallic Chemistry, 2018, vol. 32, # 8,

5029-67-4
829-85-6
37943-90-1
Synthesis of Diphenyl-2-pyridylphosphine from 2-Iodopyridine and Diphenylphosphine
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View Lastest Price from Diphenyl-2-pyridylphosphine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Diphenyl-2-pyridylphosphine pictures 2026-09-11 Diphenyl-2-pyridylphosphine
37943-90-1
$9.00-159.00 25g 0.98 100kg Shanghai UCHEM Inc.
Diphenyl-2-pyridylphosphine   pictures 2026-08-07 Diphenyl-2-pyridylphosphine
37943-90-1
$1.00 1KG 99% 20 Tons Shaanxi Dideu Medichem Co. Ltd
Diphenyl-2-pyridylphosphine pictures 2026-06-30 Diphenyl-2-pyridylphosphine
37943-90-1
1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd
Diphenyl(2-pyridinyl)phosphine 2-Diphenylphosphinopyridine, min. 97% DPPPY/DIPHENYL-2-PYRIDYL Diphenyl-2-pyridylphosphine 97% DIPHENYL-2-PYRIDYLPHOSPHINE DPPPY/DIPHENYL-2-PYRIDYLPHOSPHINE Diphenyl-2-pyridylphosphine ,97% Diphenyl-2-pyridylphosphine(DPPPy) -2-pyridyL Diphenyl-2-pyridylphosphine, 97%, for synthesis Diphenyl-2-pyridylphosphine> Pyridine, 2-(diphenylphosphino)- diphenyl(pyridin-2-yl)phosphane Diphenyl(2-pyridyl)phosphane 2-(diphenylphosphanyl)pyridine 2-(DIPHENYLPHOSPHINO)PYRIDINE 2-Pyridyldiphenylphosphine 37943-90-1 C17H14NP Catalysis and Inorganic Chemistry Phosphorus Compounds Phosphine Ligands Mitsunobu Reaction Phosphines (Mitsunobu Reaction) Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Aromatics Chelating Agents & Ligands Phosphines Mitsunobu Reaction Phosphine Ligands Phosphines (Mitsunobu Reaction) Synthetic Organic Chemistry Catalysis and Inorganic Chemistry Phosphine Ligands Phosphorus Compounds Achiral Phosphine Aryl Phosphine