2,5-Dimethoxybenzaldehyde

2,5-Dimethoxybenzaldehyde is an organic compound and a benzaldehyde derivative. ^[1]

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Table of Contents

1. 8 relations: Benzaldehyde, Chemical synthesis, Organic compound, Substituted phenethylamine, 2C-B, 2C-C, 2C-H, 2C-I.

2. Benzaldehydes

Benzaldehyde

Benzaldehyde (C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent. 2,5-Dimethoxybenzaldehyde and Benzaldehyde are Benzaldehydes.

See 2,5-Dimethoxybenzaldehyde and Benzaldehyde

Chemical synthesis

Chemical synthesis (chemical combination) is the artificial execution of chemical reactions to obtain one or several products.

See 2,5-Dimethoxybenzaldehyde and Chemical synthesis

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 2,5-Dimethoxybenzaldehyde and Organic compound

Substituted phenethylamine

Substituted phenethylamines (or simply phenethylamines) are a chemical class of organic compounds that are based upon the phenethylamine structure; the class is composed of all the derivative compounds of phenethylamine which can be formed by replacing, or substituting, one or more hydrogen atoms in the phenethylamine core structure with substituents.

See 2,5-Dimethoxybenzaldehyde and Substituted phenethylamine

2C-B

2C-B (4-bromo-2,5-dimethoxyphenethylamine), also known as Nexus, is a synthetic psychedelic drug of the 2C family, mainly used as a recreational drug.

See 2,5-Dimethoxybenzaldehyde and 2C-B

2C-C

2C-C is a psychedelic drug of the 2C family.

See 2,5-Dimethoxybenzaldehyde and 2C-C

2C-H

2C-H (2,5-dimethoxyphenethylamine) is a lesser-known substituted phenethylamine of the 2C family.

See 2,5-Dimethoxybenzaldehyde and 2C-H

2C-I

2C-I (2,5-Dimethoxy-4-iodophenethylamine) is a phenethylamine of the 2C family with psychedelic properties, primarily used as a recreational drug.

See 2,5-Dimethoxybenzaldehyde and 2C-I

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/2,5-Dimethoxybenzaldehyde

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