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Iminostilbene, 97%, Thermo Scientific Chemicals
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Catalog number B21323.22
also known as B21323-22
Price (USD)/ Each
525.00
-
Quantity:
100 g
Price (USD)/ Each
525.00
Iminostilbene, 97%, Thermo Scientific Chemicals
Catalog numberB21323.22
Price (USD)/ Each
525.00
-
Chemical Identifiers
CAS256-96-2
IUPAC Name2-azatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,9,11,13-heptaene
Molecular FormulaC14H11N
InChI KeyLCGTWRLJTMHIQZ-UHFFFAOYSA-N
SMILESN1C2=CC=CC=C2C=CC2=CC=CC=C12
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Specifications
Specification Sheet
Specification SheetFormPowder
Assay (GC)≥96.0%
Melting Point (clear melt)195.0-204.0?C
Appearance (Color)Yellow to orange
Iminostilbene has good antioxidant effects. N-acetyl iminostilbene was synthesized by incubating iminostilbene (2.0020 g, 10.360 mmol) with acetic anhydride.
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
Iminostilbene has good antioxidant effects. N-acetyl iminostilbene was synthesized by incubating iminostilbene (2.0020 g, 10.360 mmol) with acetic anhydride.
Solubility
Soluble in ethyl acetate (25 mg/ml), water (partly), dioxane, chloroform, and DMSO.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
Iminostilbene has good antioxidant effects. N-acetyl iminostilbene was synthesized by incubating iminostilbene (2.0020 g, 10.360 mmol) with acetic anhydride.
Solubility
Soluble in ethyl acetate (25 mg/ml), water (partly), dioxane, chloroform, and DMSO.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only
General References:
- A. Knell,;D. Monti,; A. Baiker. Catalytic dehydrogenation of iminodibenzyl to iminostilbene. A comparison of potassium-promoted manganese, iron and cobalt oxide catalysts. Catalysis Letters. 1995, 31 (2), 197-207.
- J. Csetenyi,; K. M. Baker,; A. Frigerio,; P. L. Morsell. Iminostilbene—a metabolite of carbamazepine isolated from rat urine. Journal of Pharmacy and Pharmacology. 1973, 25 (4), 340-341,.