Table of Contents
15 relations: Aldehyde, Benzaldehyde, Bifunctionality, Covalent organic framework, Organic compound, Organic redox reaction, Phthalaldehyde, Phthalic acid, Polymer, Schiff base, Sommelet reaction, Structural isomer, Terephthalaldehyde, Xylene, 2,6-Diformylpyridine.
- Benzaldehydes
Aldehyde
In organic chemistry, an aldehyde is an organic compound containing a functional group with the structure.
See Isophthalaldehyde and Aldehyde
Benzaldehyde
Benzaldehyde (C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent. Isophthalaldehyde and Benzaldehyde are Benzaldehydes.
See Isophthalaldehyde and Benzaldehyde
Bifunctionality
In chemistry, bifunctionality or difunctionality is the presence of two functional groups in a molecule.
See Isophthalaldehyde and Bifunctionality
Covalent organic framework
Covalent organic frameworks (COFs) are a class of porous polymers that form two- or three-dimensional structures through reactions between organic precursors resulting in strong, covalent bonds to afford porous, stable, and crystalline materials.
See Isophthalaldehyde and Covalent organic framework
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 Isophthalaldehyde 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 Isophthalaldehyde and Organic redox reaction
Phthalaldehyde
Phthalaldehyde (sometimes also o-phthalaldehyde or ortho-phthalaldehyde, OPA) is the chemical compound with the formula C6H4(CHO)2. Isophthalaldehyde and Phthalaldehyde are Benzaldehydes.
See Isophthalaldehyde and Phthalaldehyde
Phthalic acid
In organic chemistry, phthalic acid is an aromatic dicarboxylic acid, with formula and structure.
See Isophthalaldehyde and Phthalic acid
Polymer
A polymer is a substance or material consisting of very large molecules linked together into chains of repeating subunits.
See Isophthalaldehyde and Polymer
Schiff base
In organic chemistry, a Schiff base (named after Hugo Schiff) is a compound with the general structure (.
See Isophthalaldehyde and Schiff base
Sommelet reaction
The Sommelet reaction is an organic reaction in which a benzyl halide is converted to an aldehyde by action of hexamine and water.
See Isophthalaldehyde and Sommelet reaction
Structural isomer
In chemistry, a structural isomer (or constitutional isomer in the IUPAC nomenclature) of a compound is another compound whose molecule has the same number of atoms of each element, but with logically distinct bonds between them.
See Isophthalaldehyde and Structural isomer
Terephthalaldehyde
Terephthalaldehyde (TA) is an organic compound with the formula C6H4(CHO)2. Isophthalaldehyde and Terephthalaldehyde are Benzaldehydes.
See Isophthalaldehyde and Terephthalaldehyde
Xylene
In organic chemistry, xylene or xylol (IUPAC name: dimethylbenzene) are any of three organic compounds with the formula.
See Isophthalaldehyde and Xylene
2,6-Diformylpyridine
2,6-Diformylpyridine is an organic compound with the formula C5H3N(CHO)2, and typically appears as a solid powder at room temperature.
See Isophthalaldehyde and 2,6-Diformylpyridine
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