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2-Allylphenol, 98+%
2-Allylphenol, 98+%
2-Allylphenol, 98+%
Thermo Scientific Chemicals

2-Allylphenol, 98+%

CAS: 1745-81-9 | C9H10O | 134.178 g/mol
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数量:
100 g
500 g
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製品番号（カタログ番号） A10755.22
または、製品番号A10755-22
価格（JPY）
-
数量:
100 g
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化学物質識別子
CAS1745-81-9
IUPAC Name2-(prop-2-en-1-yl)phenol
Molecular FormulaC9H10O
InChI KeyQIRNGVVZBINFMX-UHFFFAOYSA-N
SMILESOC1=CC=CC=C1CC=C
さらに表示
仕様Specification Sheetスペックシート
Appearance (Color)Clear colorless to yellow
Assay (GC)≥98.0%
Refractive Index1.5440-1.5480 @ 20?C
FormLiquid
2-Allylphenol is an protected intermediate in the synthesis of metabolites of Diclofenac (D436450), a nonsteroidal anti-inflammatory compound an decycloxygenase (COX) inhibitor.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Allylphenol is an protected intermediate in the synthesis of metabolites of Diclofenac (D436450), a nonsteroidal anti-inflammatory compound an decycloxygenase (COX) inhibitor.

Solubility
Soluble in water(7 g/L).

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents and bases.
RUO – Research Use Only

General References:

  1. Daniele Reyx; Irene Campistron; Christophe Caillaud; Martine Villatte; Annick Cavedon. Thermal reaction between N-phenylmaleimide and 2-allylphenol as a model for the crosslinking reaction in bismaleimide polymerization with diallylbisphenol A. Macromolecular Chemistry and Physics. 1995, 196, (3),775-785
  2. Ted Schaefer; Rudy Sebastian; Timothy A.Wildman. The allyl and benzyl groups as hydrogen bond acceptors in derivatives of 2-allylphenol and 2-benzylphenol. Canadian Journal of Chemistry. 1979, 57, (22),3005-3009
  3. Undergoes phosphine-free Pd-catalyzed cross-coupling with vinylic halides and triflates to give dihydrobenzopyrans: Tetrahedron Lett., 39, 237 (1998); for reaction scheme, see Palladium(II) acetate, 10516.