3,4,5-Trimethoxybenzaldehyde

3,4,5-Trimethoxybenzaldehyde is an organic compound and a biochemical. ^[1]

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Table of Contents

1. 22 relations: Acyl chloride, Aldehyde, Archiv der Pharmazie, Aromaticity, Bromine, Chemical synthesis, Eudesmic acid, Methyl group, Nucleophilic substitution, Organic compound, Organic redox reaction, Organic synthesis, P-Cresol, Psychedelic drug, Rosenmund reduction, Sodium methoxide, Substituted phenethylamine, Substitution reaction, Tretoquinol, Trimazosin, Trimethoprim, Vanillin.

2. Benzaldehydes

Acyl chloride

In organic chemistry, an acyl chloride (or acid chloride) is an organic compound with the functional group.

See 3,4,5-Trimethoxybenzaldehyde and Acyl chloride

Aldehyde

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

See 3,4,5-Trimethoxybenzaldehyde and Aldehyde

Archiv der Pharmazie

The Archiv der Pharmazie (German pronunciation:, English: Archive of Pharmacy) is a monthly peer-reviewed scientific journal covering all aspects of chemistry in the life sciences.

See 3,4,5-Trimethoxybenzaldehyde and Archiv der Pharmazie

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 3,4,5-Trimethoxybenzaldehyde and Aromaticity

Bromine

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

See 3,4,5-Trimethoxybenzaldehyde and Bromine

Chemical synthesis

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

See 3,4,5-Trimethoxybenzaldehyde and Chemical synthesis

Eudesmic acid

Eudesmic acid is an O-methylated trihydroxybenzoic acid.

See 3,4,5-Trimethoxybenzaldehyde and Eudesmic acid

Methyl group

In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula (whereas normal methane has the formula). In formulas, the group is often abbreviated as Me.

See 3,4,5-Trimethoxybenzaldehyde and Methyl group

Nucleophilic substitution

In chemistry, a nucleophilic substitution (SN) is a class of chemical reactions in which an electron-rich chemical species (known as a nucleophile) replaces a functional group within another electron-deficient molecule (known as the electrophile).

See 3,4,5-Trimethoxybenzaldehyde and Nucleophilic substitution

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 3,4,5-Trimethoxybenzaldehyde and Organic compound

Organic redox reaction

Organic reductions or organic oxidations or organic redox reactions are redox reactions that take place with organic compounds.

See 3,4,5-Trimethoxybenzaldehyde and Organic redox reaction

Organic synthesis

Organic synthesis is a branch of chemical synthesis concerned with the construction of organic compounds.

See 3,4,5-Trimethoxybenzaldehyde and Organic synthesis

P-Cresol

para-Cresol, also 4-methylphenol, is an organic compound with the formula CH3C6H4(OH).

See 3,4,5-Trimethoxybenzaldehyde and P-Cresol

Psychedelic drug

Psychedelics are a subclass of hallucinogenic drugs whose primary effect is to trigger non-ordinary mental states (known as psychedelic experiences or "trips") and a perceived "expansion of consciousness".

See 3,4,5-Trimethoxybenzaldehyde and Psychedelic drug

Rosenmund reduction

The Rosenmund reduction is a hydrogenation process in which an acyl chloride is selectively reduced to an aldehyde.

See 3,4,5-Trimethoxybenzaldehyde and Rosenmund reduction

Sodium methoxide

Sodium methoxide is the simplest sodium alkoxide.

See 3,4,5-Trimethoxybenzaldehyde and Sodium methoxide

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 3,4,5-Trimethoxybenzaldehyde and Substituted phenethylamine

Substitution reaction

A substitution reaction (also known as single displacement reaction or single substitution reaction) is a chemical reaction during which one functional group in a chemical compound is replaced by another functional group.

See 3,4,5-Trimethoxybenzaldehyde and Substitution reaction

Tretoquinol

Tretoquinol is a beta-adrenergic agonist.

See 3,4,5-Trimethoxybenzaldehyde and Tretoquinol

Trimazosin

Trimazosin is a sympatholytic alpha-1 blocker. 3,4,5-Trimethoxybenzaldehyde and Trimazosin are Phenol ethers.

See 3,4,5-Trimethoxybenzaldehyde and Trimazosin

Trimethoprim

Trimethoprim (TMP) is an antibiotic used mainly in the treatment of bladder infections. 3,4,5-Trimethoxybenzaldehyde and Trimethoprim are Phenol ethers.

See 3,4,5-Trimethoxybenzaldehyde and Trimethoprim

Vanillin

Vanillin is an organic compound with the molecular formula.

See 3,4,5-Trimethoxybenzaldehyde and Vanillin

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/3,4,5-Trimethoxybenzaldehyde

Also known as Trimethoxybenzaldehyde.

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