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Merck
CN

715034

3-(二苯基膦)丙酸

97%, solid

别名:

(2-Carboxyethyl)diphenylphosphine, 4,4-Diphenyl-4-phosphabutanoic acid

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关于此项目

经验公式(希尔记法):
C15H15O2P
化学文摘社编号:
分子量:
258.25
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22
MDL number:
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产品名称

3-(二苯基膦)丙酸, 97%

SMILES string

OC(=O)CCP(c1ccccc1)c2ccccc2

InChI key

OTSIFUHGOBFOTH-UHFFFAOYSA-N

InChI

1S/C15H15O2P/c16-15(17)11-12-18(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10H,11-12H2,(H,16,17)

assay

97%

form

solid

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

mp

130-134 °C

functional group

phosphine

Quality Level

Application

Reactant for:
  • Organocatalytic asymmetric aziridination of imines and diazo compounds
  • Phosphine-mediated conversion of azides into diazo compounds
  • Preparation of rhodium catalysts for hydroformylation
  • Synthesis of reagents for the Mitsunobu reaction

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

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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Dania Ahmed et al.
AMB Express, 7(1), 210-210 (2017-11-23)
Biofilm formation by pathogenic bacteria is one of the major threats in hospital related infections, hence inhibiting and eradicating biofilms has become a primary target for developing new anti-infection approaches. The present study was aimed to develop novel antibiofilm agents

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