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43162

2-(Diphenylphosphino)ethylamine

≥95.0% (GC), liquid

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Synonym(s):

(2-Aminoethyl)diphenylphosphine, 1-Amino-2-(diphenylphosphino)ethane

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About This Item

Empirical Formula (Hill Notation):
C14H16NP
CAS Number:
4848-43-5
Molecular Weight:
229.26
NACRES:
NA.22
PubChem Substance ID:
57650168
UNSPSC Code:
12352116
MDL number:
MFCD00233831
Beilstein/REAXYS Number:
644931
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Product Name

2-(Diphenylphosphino)ethylamine, ≥95.0% (GC)

Quality Segment

100

assay

≥95.0% (GC)

form

liquid

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: ligand

greener alternative product characteristics

Catalysis
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functional group

phosphine

greener alternative category

Aligned

SMILES string

NCCP(c1ccccc1)c2ccccc2

InChI

1S/C14H16NP/c15-11-12-16(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10H,11-12,15H2

InChI key

RXEPBCWNHKZECN-UHFFFAOYSA-N

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of the 12 Principles of Green Chemistry. This product features an advanced catalyst system with unique mechanistic properties and broad substrate scope, enabling efficient transformations across diverse chemical structures. By expanding reaction versatility while reducing waste and byproduct formation, this catalyst simplifies synthesis workflows and minimizes environmental impact. Click here for more information.
2-(Diphenylphosphino)ethylamine is a phosphine ligand that has a bidentate structure with the phosphorus atom donating two lone pair electrons to coordinate with metal atoms. It is used as a reactant to synthesize active catalyst for the selective hydrogenation of amides. In addition, it is also used as a precursor to synthesize other phosphine ligands.

Application

2-(Diphenylphosphino)ethylamine can be used as a bidentate ligand in the nickel catalyst system for the reductive [2+2] cycloaddition reaction to synthesize cyclobutenes from alkynes.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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