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Anisil, 98+%, Thermo Scientific Chemicals
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Catalog number A10594.22
also known as A10594-22
Price (USD)/ Each
740.00
-
Quantity:
100 g
Price (USD)/ Each
740.00
Anisil, 98+%, Thermo Scientific Chemicals
Catalog numberA10594.22
Price (USD)/ Each
740.00
-
Chemical Identifiers
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
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Specifications
Specification Sheet
Specification SheetMelting 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.
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:
- Badathala, V. Acid treated clays: preparation, characterization and catalytic activity for synthesis of quinoxaline derivatives. J. Porous Mater. 2015, 22 (3), 779-786.
- 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.