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Merck
CN

336904

乙基二苯基膦

98%, liquid

别名:

乙二苯膦

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线性分子式:
(C6H5)2PCH2CH3
化学文摘社编号:
607-01-2
分子量:
214.24
NACRES:
NA.22
PubChem Substance ID:
24860439
UNSPSC Code:
12352002
MDL number:
MFCD00015170
Beilstein/REAXYS Number:
744253

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产品名称

乙基二苯基膦, 98%

InChI

1S/C14H15P/c1-2-15(13-9-5-3-6-10-13)14-11-7-4-8-12-14/h3-12H,2H2,1H3

SMILES string

CCP(c1ccccc1)c2ccccc2

InChI key

WUOIAOOSKMHJOV-UHFFFAOYSA-N

assay

98%

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

refractive index

n20/D 1.614 (lit.)

bp

293 °C (lit.)

density

1.048 g/mL at 25 °C (lit.)

functional group

phosphine

Quality Level

100

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相关类别

Application

Catalyst for:
  • Three component coupling reactions of arylaldehydes with Me vinyl ketone and phthalimide
  • Regio- and stereoselective hydroalkynylation of methylenecyclopropanes
  • Synthesis of oxazolidines, thiazolidines, pyrrolidines, and indoles
  • Dimer to monomer conversion
  • Tandem Morita-Baylis-Hillman/Michael addition reactions
  • Platinum-catalyzed cyclization
  • Regioselective and stereoselective [3+2] cycloaddition
  • Platinum-catalyzed intermolecular hydroamination
  • Hydroformylation reactions

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

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

法规信息

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分析证书(COA)

Lot/Batch Number
STBL3339
STBJ8952
STBH3947
STBG2884V
1440839V

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Xian B Powers et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(10), 2491-2496 (2018-12-24)
Carbon disulfide is cleaved by n-propyldiphenylphosphine and nickel(II) bromide in a one-step process, to form two unprecedented complexes: orange, [Ni(S2 C2 (Pn PrPh2 )2 )Br(Pn PrPh2 )]Br⋅CS2 (1) and purple [Ni{η2 -SC(Pn PrPh2 )2 }Br(Pn PrPh2 )]Br⋅0.5CS2 (2). Orange (1)

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