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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:
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:
Reactant for:
- 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
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
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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