Anisil, 98+%
Anisil, 98+%
Anisil, 98+%
Thermo Scientific Chemicals

Anisil, 98+%

CAS: 1226-42-2 | C16H14O4 | 270.284 g/mol
数量:
5 g
25 g
100 g
製品番号(カタログ番号) A10594.14
または、製品番号A10594-14
価格(JPY)
-
数量:
25 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS1226-42-2
IUPAC Namebis(4-methoxyphenyl)ethane-1,2-dione
Molecular FormulaC16H14O4
InChI KeyYNANGXWUZWWFKX-UHFFFAOYSA-N
SMILESCOC1=CC=C(C=C1)C(=O)C(=O)C1=CC=C(OC)C=C1
さらに表示
Melting Point (clear melt)131-135?C
Appearance (Color)Yellow
Assay (GC)≥98.0%
FormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Anisil is a biochemical utilized in the preparation of substituted bis(dithiolene)nickel complex. Further, it is used in the preparation of 3-[4,5-bis-(4-methoxy-phenyl)-1H-imidazol-2-yl]-pyridine by reacting with pyridine-3-carbaldehyde.

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
Anisil is a biochemical utilized in the preparation of substituted bis(dithiolene)nickel complex. Further, it is used in the preparation of 3-[4,5-bis-(4-methoxy-phenyl)-1H-imidazol-2-yl]-pyridine by reacting with pyridine-3-carbaldehyde.

Solubility
Insoluble in water.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Badathala, V. Acid treated clays: preparation, characterization and catalytic activity for synthesis of quinoxaline derivatives. J. Porous Mater. 2015, 22 (3), 779-786.
  2. Mastalerz, M.; Sieste, S.; Cenić, M.; Oppel, I. M. Two-Step Synthesis of Hexaammonium Triptycene: An Air-Stable Building Block for Condensation Reactions to Extended Triptycene Derivatives. J. Org. Chem. 2011, 76 (15), 6389-6393.