Diphenyl-2-pyridylphos­phine CAS 37943-90-1

• Iden­ti­fi­ca­tion
• Prop­er­ties
• Safe­ty Data
• Spec­i­fi­ca­tions & Oth­er Information
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Iden­ti­fi­ca­tion

CAS Number

37943-90-1

Name

Diphenyl-2-pyridylphos­phine

Syn­onyms

2-(Diphenylphosphino)pyridin [Ger­man] [ACD/IUPAC Name]
2-(Diphenylphosphino)pyridine [ACD/IUPAC Name]
2-(Diphénylphosphino)pyridine [French] [ACD/IUPAC Name]
2-diphenylphos­phanyl-pyri­­dine
2-diphenylphos­phinopy­­ri­­dine
2-pyridyldiphenylphos­phine
37943-90-1 [RN]
diphenyl(2-pyridinyl)phosphine
Diphenyl-2-pyridylphos­phine [Wiki]
MFCD00192108 [MDL num­ber]
Pyri­dine, 2-(diphenylphosphino)- [ACD/​Index Name]
2-(diphenylphosphanyl)pyridine
2-(Diphenylphosphino)pyridine|2-(Diphenylphosphanyl)pyridine
98%
bisphenyl-(pyridin-2-yl)phosphine
Diphenyl 2-pyridyl phos­phine
diphenyl(2-pyridyl)phosphine
diphenyl(pyridin-2-yl)phosphane
diphenylphos­phi­no-pyri­­dine
diphenylpyridinylphos­phine
DPP­PY
OR-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

Pre­cau­tion­ary Statements

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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