Pyridine-4-carboxaldehyde, 97%
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Pyridine-4-carboxaldehyde, 97%
Pyridine-4-carboxaldehyde, 97%
Pyridine-4-carboxaldehyde, 97%
Thermo Scientific Chemicals

Pyridine-4-carboxaldehyde, 97%

CAS: 872-85-5 | C6H5NO | 107.112 g/mol
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Catalog number A10656.14
also known as A10656-14
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Quantity:
25 g
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Price (USD)
44.65
Online Exclusive
49.50
Save 4.85 (10%)
Each
Add to cart
Chemical Identifiers
CAS872-85-5
IUPAC Namepyridine-4-carbaldehyde
Molecular FormulaC6H5NO
InChI KeyBGUWFUQJCDRPTL-UHFFFAOYSA-N
SMILESO=CC1=CC=NC=C1
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SpecificationsSpecification SheetSpecification Sheet
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to yellow to brown
FormLiquid
Assay (GC)≥96.0%
Refractive Index1.5415-1.5465 @ 20?C
Pyridine-4-carboxaldehyde is an heterocyclic building block used for the synthesis of various pharmaceutical compounds, such as new 1,4-dihydropyridin-4-yl-phenoxyacetohydrazones, having anticonvulsant and anti-inflammatory properties.

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
Pyridine-4-carboxaldehyde is an heterocyclic building block used for the synthesis of various pharmaceutical compounds, such as new 1,4-dihydropyridin-4-yl-phenoxyacetohydrazones, having anticonvulsant and anti-inflammatory properties.

Solubility
Soluble in water (20 mg/ml at 20°C), ethanol and acetone.

Notes
It is air and light sensitive. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Nand K.Singh; Rajesh Tripathi. Synthesis and structural characterization of 3d-metal complexes of pyridine-4-carboxaldehyde thionicotinoyl hydrazone. Transition Metal Chemistry. 1988, 13, (5),346-350
  2. A.Martin; B.Lucke; H.J.Niclas; A.Forster. Vapor-phase oxidation of 4-picoline to pyridine-4-carboxaldehyde on a vanadium phosphate catalysts. Reaction Kinetics and Catalysis Letters. 1991, 43, (2),583-588
  3. In the presence of DBU, converts amines to carbonyl compounds, e.g. benzylamines to benzaldehydes: Synthesis, 756 (1982):
  4. The reaction is also useful for the conversion of ɑ-amino acids to ɑ-keto acids.