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53014-84-9

6-methylpyridine-3-carbaldehyde

CAS: 53014-84-9

Molecular Formula: C7H7NO

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53014-84-9 - Names and Identifiers

Name 6-methylpyridine-3-carbaldehyde
Synonyms 5-FORMYL-2-PICOLINE
6-Methylnicotinaldehyde
5-Formyl-2-methylpyridine
3-Formyl-6-Methyl-Pyridine
3-FORMYL-6-METHYL-PYRIDINE
6-methylpyridine-3-carbaldehyde
6-METHYL-3-PYRIDINECARBOXALDEHYDE
6-Methylpyridine-3-carboxaldehyde
3-Pyridinecarboxaldehyde, 6-methyl-
CAS 53014-84-9
InChI InChI=1/C7H7NO/c1-6-2-3-7(5-9)4-8-6/h2-5H,1H3
InChIKey IMWMEIWYPWVABQ-UHFFFAOYSA-N

53014-84-9 - Physico-chemical Properties

Molecular FormulaC7H7NO
Molar Mass121.14
Density1.084
Boling Point95℃/20mm
Flash Point88℃
Vapor Presure0.162mmHg at 25°C
AppearanceLiquid
pKa4.15±0.10(Predicted)
Storage Conditionunder inert gas (nitrogen or Argon) at 2-8°C
SensitiveMoisture Sensitive
Refractive Index1.546

53014-84-9 - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk CodesR22 - Harmful if swallowed
R36 - Irritating to the eyes
Safety Description26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany3
HS Code29333990

53014-84-9 - Introduction

It is an organic compound with the chemical formula C8H9NO. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
-Appearance: colorless to yellowish liquid.
-Solubility: Soluble in organic solvents, such as ethanol, chloroform and dimethylformamide.
-Melting point: approximately -2 to -4 degrees Celsius.
-Boiling point: approximately 228 to 232 degrees Celsius.

Use:
-is often used as a reagent and intermediate in organic synthesis.
-In the field of medicine, it can be used to synthesize some drugs and biologically active compounds.
-It can also be used as a precursor of organic acids and used in the synthesis of compounds containing pyridine structures in some studies.

Preparation Method:
It can be synthesized by the following methods:
-Starting from 3-amino -6-methyl pyridine, through the classic Karl Fischer reaction, the amino group is esterified by Karl Fischer antimonic acid, and then through oxidation, hydrolysis and acylation And other reaction steps, the final yield.

Safety Information:
There is currently no extensive data on toxicity or harmfulness for the safety of the process. However, as a chemical, it still needs to be handled and used properly. During use, direct contact with skin and eyes should be avoided. At the same time, when handling and storing the compound, it is necessary to follow the chemical safety procedures and take appropriate protective measures, such as wearing gloves, safety glasses and laboratory coats. In case of any accident, get medical help immediately and seek professional advice.
Last Update:2024-04-09 21:11:58
53014-84-9
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53014-84-9
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