3-Nitrobenzaldehyde

3-Nitrobenzaldehyde is an organic aromatic compound containing a nitro group meta-substituted to an aldehyde. ^[1]

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Table of Contents

1. 10 relations: Aldehyde, Aromaticity, Benzaldehyde, Calcium channel blocker, Functional group, Nitration, Nitric acid, Nitro compound, Tipranavir, 1,4-Dihydropyridine.

2. Benzaldehydes

Aldehyde

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

See 3-Nitrobenzaldehyde and Aldehyde

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.

See 3-Nitrobenzaldehyde and Aromaticity

Benzaldehyde

Benzaldehyde (C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent. 3-Nitrobenzaldehyde and Benzaldehyde are Benzaldehydes.

See 3-Nitrobenzaldehyde and Benzaldehyde

Calcium channel blocker

Calcium channel blockers (CCB), calcium channel antagonists or calcium antagonists are a group of medications that disrupt the movement of calcium through calcium channels.

See 3-Nitrobenzaldehyde and Calcium channel blocker

Functional group

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

See 3-Nitrobenzaldehyde and Functional group

Nitration

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

See 3-Nitrobenzaldehyde and Nitration

Nitric acid

Nitric acid is the inorganic compound with the formula.

See 3-Nitrobenzaldehyde and Nitric acid

Nitro compound

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

See 3-Nitrobenzaldehyde and Nitro compound

Tipranavir

Tipranavir (TPV), or tipranavir disodium, is a nonpeptidic protease inhibitor (PI) manufactured by Boehringer Ingelheim under the trade name Aptivus.

See 3-Nitrobenzaldehyde and Tipranavir

1,4-Dihydropyridine

1,4-Dihydropyridine (DHP) is an organic compound with the formula CH2(CH.

See 3-Nitrobenzaldehyde and 1,4-Dihydropyridine

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/3-Nitrobenzaldehyde

Also known as M-nitrobenzaldehyde.

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