Pyridine-2-carboxaldehyde, 99%
Pyridine-2-carboxaldehyde, 99%
Pyridine-2-carboxaldehyde, 99%
Pyridine-2-carboxaldehyde, 99%
Thermo Scientific Chemicals

Pyridine-2-carboxaldehyde, 99%

CAS: 1121-60-4 | C6H5NO | 107.112 g/mol
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Catalog NumberQuantity
ALFA11391.1425 g
Catalog number ALFA11391.14
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25 g
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Specifications
Chemical Name or MaterialPyridine-2-carboxaldehyde
CAS1121-60-4
Health Hazard 1H227-H302-H315-H318-H331
Health Hazard 2GHS H Statement
H331-H318-H227-H302-H315-H317-H335
Toxic if inhaled.
Causes serious eye damage.
Combustible liquid.
Harmful if swallowed.
Causes skin irritation.
May cause an allergic skin reaction.
May cause respiratory irritation.
Health Hazard 3P210-P235-P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P310-P311-P330-P332+P313-P362-P370+P378q-P501c
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Pyridine-2-carboxaldehyde, 99% is used as an Intermediate of Bisacodyl. It is also used as an intermediate in pharamceutical research, Intermediate in organicc synethesis.

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-2-carboxaldehyde, 99% is used as an Intermediate of Bisacodyl. It is also used as an intermediate in pharamceutical research, Intermediate in organicc synethesis.

Solubility
It is soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature 2 - 8°C .Store under inert gas. Stable under recommended storage conditions.Incompatible to Strong bases, Strong oxidizing agents and acids.
RUO – Research Use Only

General References:

  1. Anthony J. Mancuso.; Debra S. Brownfain.; Daniel Swern. Structure of the dimethyl sulfoxide-oxalyl chloride reaction product. Oxidation of heteroaromatic and diverse alcohols to carbonyl compounds. J. Org. Chem. 1979, 44, (23), 4148-4150.
  2. Lorenzo Testaferri.; Marco Tingoli.; Marcello Tiecco. Reactions of polychlorobenzenes with alkanethiol anions in HMPA. A simple, high-yield synthesis of poly(alkylthio)benzenes. J. Org. Chem. 1980, 45, (22), 4376-4380.
  3. Has been applied in a sequence for the oxidative deamination of amines to ketones, by reaction of the imines with mCPBA and cleavage of the resulting oxaziridines: J. Am. Chem. Soc., 97, 6900 (1975):