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Thermo Scientific Chemicals
Pyridine-2-carboxaldehyde, 99%
CAS: 1121-60-4 | C6H5NO | 107.112 g/mol
化学物質識別子
CAS1121-60-4
IUPAC Namepyridine-2-carbaldehyde
Molecular FormulaC6H5NO
InChI KeyCSDSSGBPEUDDEE-UHFFFAOYSA-N
SMILESO=CC1=CC=CC=N1
さらに表示
仕様
スペックシート
スペックシートAssay (GC)≥98.5%
Free acid (titration)<1.0%
Identification (FTIR)Conforms
Refractive Index1.5345-1.5385 @ 20°C
Appearance (Color)Clear colorless to dark yellow or brown
さらに表示
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.
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:
- 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.
- 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.
- 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):