N-Acetonylpyridinium chloride, 97%, Thermo Scientific Chemicals
N-Acetonylpyridinium chloride, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

N-Acetonylpyridinium chloride, 97%, Thermo Scientific Chemicals

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Quantity:
25 g
5 g
Catalog number A16015.14
also known as A16015-14
Price (USD)/ Each
208.00
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Quantity:
25 g
Request bulk or custom format
Price (USD)/ Each
208.00
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N-Acetonylpyridinium chloride, 97%, Thermo Scientific Chemicals
Catalog numberA16015.14
Price (USD)/ Each
208.00
-
Add to cart
Chemical Identifiers
CAS42508-60-1
IUPAC Name1-(2-oxopropyl)pyridin-1-ium chloride
Molecular FormulaC8H10ClNO
InChI KeyJHYYWKUENNZTMD-UHFFFAOYSA-M
SMILES[Cl-].CC(=O)C[N+]1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder
Melting Point (clear melt)201.0-210.0?C
Appearance (Color)Cream to pale brown
Assay (Titration ex Chloride)≥96.0 to ≤104.0%
N-Acetonylpyridinium chloride is used as a pharmaceutical intermediate.

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
N-Acetonylpyridinium chloride is used as a pharmaceutical intermediate.

Solubility
Soluble in water.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents. Store under dry inert gas. It is hygroscopic in nature. Protect from water and humidity.
RUO – Research Use Only

General References:

  1. Tuyen Nguyen Van, Guido Verniest, Sven Claessens, Norbert De Kimpe. Total synthesis of four naturally occurring 2-azaanthraquinone antibiotics, 6-deoxy-8-methylbostrycoidin, 6-deoxybostrycoidin, 7-O-demethyl-6-deoxybostrycoidin and scorpinone. Tetrahedron. 2005, 61 (9), 2295-2300.
  2. Margaret A. Brimble.; Scott I. Houghton.; Paul D. Woodgate. Synthesis of a regioisomeric analogue of the 3C-protease inhibitor thysanone via a Hauser annulation strategy. Tetrahedron. 2007, 63 (4), 880-887.