Table of Contents
19 relations: Alkylbenzene, Ammoxidation, Butadiene, Cyclic compound, Dehydrogenation, Isomer, Isomerization, Methyl group, Monomer, Naphthalene, O-Xylene, Petroleum, Polycyclic aromatic hydrocarbon, Polyethylene terephthalate, Polymer, Redox, Sodium–potassium alloy, Thermal conductance and resistance, 2,6-Naphthalenedicarboxylic acid.
- Aromatic hydrocarbons
Alkylbenzene
An alkylbenzene is a chemical compound that contains a monocyclic aromatic ring attaching to one or more saturated hydrocarbon chains.
See 2,6-Dimethylnaphthalene and Alkylbenzene
Ammoxidation
In organic chemistry, ammoxidation is a process for the production of nitriles using ammonia and oxygen.
See 2,6-Dimethylnaphthalene and Ammoxidation
Butadiene
1,3-Butadiene is the organic compound with the formula CH2.
See 2,6-Dimethylnaphthalene and Butadiene
Cyclic compound
A cyclic compound (or ring compound) is a term for a compound in the field of chemistry in which one or more series of atoms in the compound is connected to form a ring.
See 2,6-Dimethylnaphthalene and Cyclic compound
Dehydrogenation
In chemistry, dehydrogenation is a chemical reaction that involves the removal of hydrogen, usually from an organic molecule.
See 2,6-Dimethylnaphthalene and Dehydrogenation
Isomer
In chemistry, isomers are molecules or polyatomic ions with identical molecular formula – that is, the same number of atoms of each element – but distinct arrangements of atoms in space.
See 2,6-Dimethylnaphthalene and Isomer
Isomerization
In chemistry, isomerization or isomerisation is the process in which a molecule, polyatomic ion or molecular fragment is transformed into an isomer with a different chemical structure.
See 2,6-Dimethylnaphthalene and Isomerization
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 2,6-Dimethylnaphthalene and Methyl group
Monomer
A monomer (mono-, "one" + -mer, "part") is a molecule that can react together with other monomer molecules to form a larger polymer chain or three-dimensional network in a process called polymerization.
See 2,6-Dimethylnaphthalene and Monomer
Naphthalene
Naphthalene is an organic compound with formula. 2,6-Dimethylnaphthalene and Naphthalene are Naphthalenes.
See 2,6-Dimethylnaphthalene and Naphthalene
O-Xylene
o-Xylene (ortho-xylene) is an aromatic hydrocarbon with the formula C6H4(CH3)2, with two methyl substituents bonded to adjacent carbon atoms of a benzene ring (the ortho configuration).
See 2,6-Dimethylnaphthalene and O-Xylene
Petroleum
Petroleum or crude oil, also referred to as simply oil, is a naturally occurring yellowish-black liquid mixture of mainly hydrocarbons, and is found in geological formations.
See 2,6-Dimethylnaphthalene and Petroleum
Polycyclic aromatic hydrocarbon
A polycyclic aromatic hydrocarbon (PAH) is a class of organic compounds that is composed of multiple aromatic rings.
See 2,6-Dimethylnaphthalene and Polycyclic aromatic hydrocarbon
Polyethylene terephthalate
Polyethylene terephthalate (or poly(ethylene terephthalate), PET, PETE, or the obsolete PETP or PET-P), is the most common thermoplastic polymer resin of the polyester family and is used in fibres for clothing, containers for liquids and foods, and thermoforming for manufacturing, and in combination with glass fibre for engineering resins.
See 2,6-Dimethylnaphthalene and Polyethylene terephthalate
Polymer
A polymer is a substance or material consisting of very large molecules linked together into chains of repeating subunits.
See 2,6-Dimethylnaphthalene and Polymer
Redox
Redox (reduction–oxidation or oxidation–reduction) is a type of chemical reaction in which the oxidation states of the reactants change.
See 2,6-Dimethylnaphthalene and Redox
Sodium–potassium alloy
Sodium–potassium alloy, colloquially called NaK (commonly pronounced), is an alloy of the alkali metals sodium (Na, atomic number 11) and potassium (K, atomic number 19) that is normally liquid at room temperature.
See 2,6-Dimethylnaphthalene and Sodium–potassium alloy
Thermal conductance and resistance
In heat transfer, thermal engineering, and thermodynamics, thermal conductance and thermal resistance are fundamental concepts that describe the ability of materials or systems to conduct heat and the opposition they offer to the heat current.
See 2,6-Dimethylnaphthalene and Thermal conductance and resistance
2,6-Naphthalenedicarboxylic acid
2,6-Naphthalenedicarboxylic acid is an organic compound with the formula C10H6(CO2H)2. 2,6-Dimethylnaphthalene and 2,6-Naphthalenedicarboxylic acid are Naphthalenes.
See 2,6-Dimethylnaphthalene and 2,6-Naphthalenedicarboxylic acid
See also
Aromatic hydrocarbons
- 1,1'-Binaphthyl
- 1,2,3,4,5-Pentakis(4-butylphenyl)-1,3-cyclopentadiene
- 1,4-Dimethylnaphthalene
- 1,5-Methano(10)annulene
- 1,6-Methano(10)annulene
- 1-Methylnaphthalene
- 1-Nonylnaphthalene
- 2,6-Diisopropylnaphthalene
- 2,6-Dimethylnaphthalene
- 2-Methylnaphthalene
- Alkylbenzenes
- Annulenes
- Arylene
- Aryne
- Benzene
- Benzene derivatives
- Diisopropylnaphthalenes
- Gomberg's dimer
- Hexaphenylethane
- M-Terphenyl
- Polycyclic aromatic hydrocarbons
- Terphenyl
- Tetralin
- Tetraphenylethylene
- Tetraphenylmethane
- Thermal rearrangement of aromatic hydrocarbons
- Trans-Propenylbenzene
- Triphenylmethane
References
Also known as 2,6-dimethylnaphtalene.