4-Bromobenzaldehyde

4-Bromobenzaldehyde, or p-bromobenzaldehyde, is an organobromine compound with the formula. ^[1]

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Table of Contents

1. 15 relations: Bromine, Bromobenzaldehyde, Bromotoluene, Calcium carbonate, ChemSpider, Cross-coupling reaction, Free-radical halogenation, Journal of the American Chemical Society, Organic Syntheses, Organobromine chemistry, Sonogashira coupling, Suzuki reaction, Trimethylsilylacetylene, 3-Bromobenzaldehyde, 4-Ethynylbenzaldehyde.

2. Benzaldehydes

Bromine

Bromine is a chemical element; it has symbol Br and atomic number 35.

See 4-Bromobenzaldehyde and Bromine

Bromobenzaldehyde

Bromobenzaldehydes are any of three organic compounds with the formula BrC6H4COH, consisting of a formyl group and a bromine atom attached to a central benzene ring. 4-Bromobenzaldehyde and Bromobenzaldehyde are Benzaldehydes and Bromobenzene derivatives.

See 4-Bromobenzaldehyde and Bromobenzaldehyde

Bromotoluene

Bromotoluenes are aryl bromides based on toluene in which at least one aromatic hydrogen atom is replaced with a bromine atom. 4-Bromobenzaldehyde and Bromotoluene are Bromobenzene derivatives.

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Calcium carbonate

Calcium carbonate is a chemical compound with the chemical formula.

See 4-Bromobenzaldehyde and Calcium carbonate

ChemSpider

ChemSpider is a freely accessible online database of chemicals owned by the Royal Society of Chemistry.

See 4-Bromobenzaldehyde and ChemSpider

Cross-coupling reaction

In organic chemistry, a cross-coupling reaction is a reaction where two different fragments are joined.

See 4-Bromobenzaldehyde and Cross-coupling reaction

Free-radical halogenation

In organic chemistry, free-radical halogenation is a type of halogenation.

See 4-Bromobenzaldehyde and Free-radical halogenation

Journal of the American Chemical Society

The Journal of the American Chemical Society (also known as JACS) is a weekly peer-reviewed scientific journal that was established in 1879 by the American Chemical Society.

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Organic Syntheses

Organic Syntheses is a peer-reviewed scientific journal that was established in 1921.

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Organobromine chemistry

Organobromine chemistry is the study of the synthesis and properties of organobromine compounds, also called organobromides, which are organic compounds that contain carbon bonded to bromine.

See 4-Bromobenzaldehyde and Organobromine chemistry

Sonogashira coupling

The Sonogashira reaction is a cross-coupling reaction used in organic synthesis to form carbon–carbon bonds.

See 4-Bromobenzaldehyde and Sonogashira coupling

Suzuki reaction

The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide.

See 4-Bromobenzaldehyde and Suzuki reaction

Trimethylsilylacetylene

Trimethylsilylacetylene is the organosilicon compound with the formula.

See 4-Bromobenzaldehyde and Trimethylsilylacetylene

3-Bromobenzaldehyde

3-Bromobenzaldehyde is an isomer of bromobenzaldehyde. 4-Bromobenzaldehyde and 3-Bromobenzaldehyde are Benzaldehydes and Bromobenzene derivatives.

See 4-Bromobenzaldehyde and 3-Bromobenzaldehyde

4-Ethynylbenzaldehyde

4-Ethynylbenzaldehyde, or p-ethynylbenzaldehyde, is an organic compound with the formula HC2C6H4COH. 4-Bromobenzaldehyde and 4-Ethynylbenzaldehyde are Benzaldehydes.

See 4-Bromobenzaldehyde and 4-Ethynylbenzaldehyde

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/4-Bromobenzaldehyde

Also known as P-Bromobenzaldehyde.

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