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Merck
CN

710369

双(2-呋喃基)氯化膦

85%

别名:

Di-2-furanylphosphinous chloride

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关于此项目

经验公式(希尔记法):
C8H6ClO2P
化学文摘社编号:
分子量:
200.56
UNSPSC Code:
12352005
PubChem Substance ID:
MDL number:
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InChI

1S/C8H6ClO2P/c9-12(7-3-1-5-10-7)8-4-2-6-11-8/h1-6H

SMILES string

ClP(c1ccco1)c2ccco2

InChI key

IYEUYNXDXNWPJI-UHFFFAOYSA-N

assay

85%

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 1.593

density

1.287 g/mL at 25 °C

functional group

phosphine

Application

Reactant for synthesis of:
  • Centrostereogenic 1,3-bidentate ferrocenyldiphosphane ligands
  • Ferrocene-based chiral diphosphine
  • Phosphine containing amino acids

Reactant for:
  • α-Arylation of aldehydes
  • Stereoselective [2,3] sigmatropic rearrangement of acyclic allylic phosphinites
  • Hydrophosphination of functionalized alkenes

pictograms

FlameCorrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B - Water-react 2

存储类别

4.3 - Hazardous materials which set free flammable gases upon contact with water

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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P M Ferreira et al.
Scientific reports, 10(1), 18061-18061 (2020-10-24)
Platelet-derived extracellular vesicles (PDEVs) are the most abundant amongst all types of EVs in the circulation. However, the mechanisms leading to PDEVs release, their role in coagulation and phenotypic composition are poorly understood. PDEVs from washed platelets were generated using

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