2-Nitrobenzaldehyde

2-Nitrobenzaldehyde is an organic aromatic compound containing a nitro group ortho to formyl. ^[1]

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Table of Contents

1. 28 relations: Acetic acid, Acetic anhydride, Acetone, Aldehyde, Aniline, Aromaticity, Baeyer–Drewsen indigo synthesis, Benzaldehyde, Bisulfite, Cinnamaldehyde, Cinnamic acid, Decarboxylation, Dimethyl sulfoxide, Functional group, Halogenation, Indigo carmine, Indigo dye, Mononitrotoluene, Nitration, Nitro compound, Photolabile protecting group, Redox, Sodium bicarbonate, Styrene, Toluene, Vinyl group, 2-Nitrocinnamaldehyde, 3-Nitrobenzaldehyde.

2. Benzaldehydes

Acetic acid

Acetic acid, systematically named ethanoic acid, is an acidic, colourless liquid and organic compound with the chemical formula (also written as,, or). Vinegar is at least 4% acetic acid by volume, making acetic acid the main component of vinegar apart from water.

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Acetic anhydride

Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula.

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Acetone

Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula.

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Aldehyde

In organic chemistry, an aldehyde is an organic compound containing a functional group with the structure.

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Aniline

Aniline (and -ine indicating a derived substance) is an organic compound with the formula.

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Aromaticity

In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected by the stabilization of conjugation alone.

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Baeyer–Drewsen indigo synthesis

The Baeyer–Drewsen indigo synthesis (1882) is an organic reaction in which indigo is prepared from 2-nitrobenzaldehyde and acetone The reaction was developed by von Baeyer and in 1880 to produce the first synthetic indigo at laboratory scale.

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Benzaldehyde

Benzaldehyde (C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent. 2-Nitrobenzaldehyde and Benzaldehyde are Benzaldehydes.

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Bisulfite

The bisulfite ion (IUPAC-recommended nomenclature: hydrogensulfite) is the ion.

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Cinnamaldehyde

Cinnamaldehyde is an organic compound with the formula C9H8O or C₆H₅CH.

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Cinnamic acid

Cinnamic acid is an organic compound with the formula C6H5-CH.

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Decarboxylation

Decarboxylation is a chemical reaction that removes a carboxyl group and releases carbon dioxide (CO2).

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Dimethyl sulfoxide

Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH3)2.

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Functional group

In organic chemistry, a functional group is a substituent or moiety in a molecule that causes the molecule's characteristic chemical reactions.

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Halogenation

In chemistry, halogenation is a chemical reaction which introduces one or more halogens into a chemical compound.

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Indigo carmine

Indigo carmine, or 5,5′-indigodisulfonic acid sodium salt, is an organic salt derived from indigo by aromatic sulfonation, which renders the compound soluble in water.

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Indigo dye

Indigo dye is an organic compound with a distinctive blue color.

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Mononitrotoluene

Mononitrotoluene or nitrotoluene (MNT or NT), is any of three organic compounds with the formula C6H4(CH3)(NO2).

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Nitration

In organic chemistry, nitration is a general class of chemical processes for the introduction of a nitro group into an organic compound.

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Nitro compound

In organic chemistry, nitro compounds are organic compounds that contain one or more nitro functional groups.

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Photolabile protecting group

A photolabile protecting group (PPG; also known as: photoremovable, photosensitive, or photocleavable protecting group) is a chemical modification to a molecule that can be removed with light.

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Redox

Redox (reduction–oxidation or oxidation–reduction) is a type of chemical reaction in which the oxidation states of the reactants change.

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Sodium bicarbonate

Sodium bicarbonate (IUPAC name: sodium hydrogencarbonate), commonly known as baking soda or bicarbonate of soda, is a chemical compound with the formula NaHCO3.

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Styrene

Styrene is an organic compound with the chemical formula C6H5CH.

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Toluene

Toluene, also known as toluol, is a substituted aromatic hydrocarbon with the chemical formula, often abbreviated as, where Ph stands for phenyl group.

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Vinyl group

In organic chemistry, a vinyl group (abbr. Vi; IUPAC name: ethenyl group) is a functional group with the formula.

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2-Nitrocinnamaldehyde

2-Nitrocinnamaldehyde, ortho-nitrocinnamaldehyde or o-nitrocinnamaldehyde is an organic aromatic compound containing a nitro group ortho- to the 1-position of cinnamaldehyde. 2-Nitrobenzaldehyde and 2-Nitrocinnamaldehyde are Nitrobenzene derivatives.

See 2-Nitrobenzaldehyde and 2-Nitrocinnamaldehyde

3-Nitrobenzaldehyde

3-Nitrobenzaldehyde is an organic aromatic compound containing a nitro group meta-substituted to an aldehyde. 2-Nitrobenzaldehyde and 3-Nitrobenzaldehyde are Benzaldehydes and Nitrobenzene derivatives.

See 2-Nitrobenzaldehyde and 3-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-Nitrobenzaldehyde

Also known as O-nitrobenzaldehyde.

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