Skip to Content
Merck
CN

381241

Diethylphenylphosphine

96%

Synonym(s):

NSC 158475

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
(C2H5)2PC6H5
CAS Number:
Molecular Weight:
166.20
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-516-6
Beilstein/REAXYS Number:
742484
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

LVTCZSBUROAWTE-UHFFFAOYSA-N

InChI

1S/C10H15P/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3

SMILES string

CCP(CC)c1ccccc1

assay

96%

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

refractive index

n20/D 1.546 (lit.)

bp

120-121 °C/29 mmHg (lit.)

density

0.954 g/mL at 25 °C (lit.)

functional group

phosphine

Quality Level

Related Categories

Application

Catalyst for:
  • Selective cross-dimerization
  • Diastereoselective condensations
  • Carboxyl migration reactions
  • Selective hydrogenation
  • Asymmetric induction by chiral diphosphines in ring contraction

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

183.2 °F - closed cup

flash_point_c

84 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

B P Smyser et al.
Biochemical pharmacology, 35(10), 1719-1723 (1986-05-15)
Purified mouse liver cytochrome P-450 reconstituted with purified NADPH-cytochrome P-450 reductase and phosphatidylcholine metabolized diethylphenylphosphine to diethylphenylphosphine oxide. NADPH was required for the reaction and the amount of oxide formed was time and cytochrome P-450 dependent. Purified phenobarbital-induced cytochrome P-450

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service