2-Aminobenzaldehyde

2-Aminobenzaldehyde is an organic compound with the formula C6H4(NH2)CHO. ^[1]

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Table of Contents

1. 9 relations: Aminoaldehydes and aminoketones, Friedländer synthesis, Iron(II) sulfate, Ligand, Organic compound, Quinoline, Self-condensation, Template reaction, 2-Nitrobenzaldehyde.

2. Benzaldehydes

Aminoaldehydes and aminoketones

Aminoaldehydes and aminoketones are organic compounds that contain an amine functional group as well as either a aldehyde or ketone functional group. 2-Aminobenzaldehyde and Aminoaldehydes and aminoketones are amines.

See 2-Aminobenzaldehyde and Aminoaldehydes and aminoketones

Friedländer synthesis

The Friedländer synthesis is a chemical reaction of 2-aminobenzaldehydes with ketones to form quinoline derivatives.

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Iron(II) sulfate

Iron(II) sulfate (British English: iron(II) sulphate) or ferrous sulfate denotes a range of salts with the formula FeSO4·xH2O.

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Ligand

In coordination chemistry, a ligand is an ion or molecule with a functional group that binds to a central metal atom to form a coordination complex.

See 2-Aminobenzaldehyde and Ligand

Organic compound

Some chemical authorities define an organic compound as a chemical compound that contains a carbon–hydrogen or carbon–carbon bond; others consider an organic compound to be any chemical compound that contains carbon.

See 2-Aminobenzaldehyde and Organic compound

Quinoline

Quinoline is a heterocyclic aromatic organic compound with the chemical formula C9H7N.

See 2-Aminobenzaldehyde and Quinoline

Self-condensation

In organic chemistry, self-condensation is an organic reaction in which a chemical compound containing a carbonyl group acts both as the electrophile and the nucleophile in an aldol condensation.

See 2-Aminobenzaldehyde and Self-condensation

Template reaction

In chemistry, a template reaction is any of a class of ligand-based reactions that occur between two or more adjacent coordination sites on a metal center.

See 2-Aminobenzaldehyde and Template reaction

2-Nitrobenzaldehyde

2-Nitrobenzaldehyde is an organic aromatic compound containing a nitro group ortho to formyl. 2-Aminobenzaldehyde and 2-Nitrobenzaldehyde are Benzaldehydes.

See 2-Aminobenzaldehyde and 2-Nitrobenzaldehyde

See also

Benzaldehydes

• 2,4-Dimethoxybenzaldehyde
• 2,5-Dimethoxybenzaldehyde
• 2-Aminobenzaldehyde
• 2-Carboxybenzaldehyde
• 2-Chloro-6-fluorobenzaldehyde
• 2-Chlorobenzaldehyde
• 2-Diphenylphosphinobenzaldehyde
• 2-Methoxybenzaldehyde
• 2-Methylbenzaldehyde
• 2-Nitrobenzaldehyde
• 3,4,5-Trimethoxybenzaldehyde
• 3-Acetyl-6-methoxybenzaldehyde
• 3-Bromobenzaldehyde
• 3-Nitrobenzaldehyde
• 4-Anisaldehyde
• 4-Bromobenzaldehyde
• 4-Carboxybenzaldehyde
• 4-Chlorobenzaldehyde
• 4-Ethylbenzaldehyde
• 4-Ethynylbenzaldehyde
• 4-Formylphenylboronic acid
• 4-Methylbenzaldehyde
• 4-Nitrobenzaldehyde
• AC-42
• Benzaldehyde
• Bromobenzaldehyde
• Casiraghi formylation
• Chlorobenzaldehyde
• Connorstictic acid
• Constictic acid
• Cuminaldehyde
• Dimethoxybenzaldehyde
• Flavipin
• Fluorobenzaldehyde
• Helicin
• Hericenone
• Hernandaline
• Isophthalaldehyde
• Mesitaldehyde
• Nemtabrutinib
• Nitrobenzaldehyde
• Para-Dimethylaminobenzaldehyde
• Phthalaldehyde
• Piperonal
• Taber's reagent
• Terephthalaldehyde
• Veratraldehyde

References

[1] https://en.wikipedia.org/wiki/2-Aminobenzaldehyde

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