573-98-8

Basic information

• Product Name: 1,2-DIMETHYLNAPHTHALENE
• Synonyms: 1,2-DIMETHYLNAPHTHALENE 96+%;1,2-DiMethylnaphthalene 95%;1,2-DIMETHYLNAPHTHALENE;Naphthalene, 1,2-dimethyl-;1,2-DIMETHYLNAPHTHALENE OEKANAL, 250 MG;1,2-Dimethylnaphthalene,98%
• CAS NO: 573-98-8
• Molecular Formula: C₁₂H₁₂
• Molecular Weight: 156.22
• EINECS: 209-364-7
• Product Categories: Naphthalene derivatives;NaphthalenesChemical Class;PAHsMore...Close...;Alpha Sort;Analytical Standards;AromaticsVolatiles/ Semivolatiles;Chemical Class;D;DAlphabetic;DID - DINAnalytical Standards;Hydrocarbons;NeatsAnalytical Standards;Arenes;Building Blocks;Organic Building Blocks
• Mol File: 573-98-8.mol
• Article Data: 22

Chemical Properties

• Melting Point: −2-−1 °C(lit.)
• Boiling Point: 266-267 °C(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.013 g/mL at 25 °C(lit.)
• Refractive Index: n20/D 1.615(lit.)
• Water Solubility: Difficult to mix in water.
• BRN: 2039376
• CAS DataBase Reference: 1,2-DIMETHYLNAPHTHALENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DIMETHYLNAPHTHALENE(573-98-8)
• EPA Substance Registry System: 1,2-DIMETHYLNAPHTHALENE(573-98-8)

Safety Data

• Safety Statements: 23-24/25
• WGK Germany: 3
• Hazardous Substances Data: 573-98-8(Hazardous Substances Data)

Usage

Uses

1,2-Dimethylnaphthalene is suitable reagent used to investigate the secondary organic aerosol (SOA) production via gas-phase photooxidation.

Definition

ChEBI: A dimethylnaphthalene carrying methyl groups at positions 1 and 2.

General Description

1,2-Dimethylnaphthalene belongs to the family of polycyclic aromatic hydrocarbons (PAHs), which are of industrial relevance. PAHs are considered as common environmental contaminants and can adversely affect human health.

InChI:InChI=1/C12H12/c1-9-7-8-11-5-3-4-6-12(11)10(9)2/h3-8H,1-2H3

Upstream product

• 6626-23-9 1-chloromethyl-2-methyl-naphthalene 
• 5195-39-1 3,4-dimethyl-1,2-dihydronaphthalene 
• 35699-44-6 2-methyl-1-naphthaldehyde 
• 1985-59-7 1,1-dimethyltetralin 
• 118-75-2 chloranil 
• 2586-62-1 1-bromo-2-methylnaphtalene 
• 77-78-1 dimethyl sulfate 
• 84-58-2 2,3-dicyano-5,6-dichloro-p-benzoquinone 
• 71-43-2 benzene 
• 638-02-8 2,5-DIMETHYLTHIOPHENE 
• 1488-42-2 Diphenyliodonium-2-carboxylate 
• 110-71-4 1,2-dimethoxyethane 
• 22303-18-0 1,1-dimethyl-1,2-dihydronaphthalen-2-ol 
• 87031-39-8 1-Amino-3,4-dimethylnaphthalene 

Downstream Products

• 61172-29-0 1-bromomethyl-2-methylnaphthalene 
• 94465-12-0 2-(3,4-Dimethyl-naphthoyl-⁽¹⁾)-benzoesaeure 
• 1706-15-6 α-methyl-1-naphthalenometanol 
• 16020-34-1 1-Hydroxy-3,4-dimethylnaphthalene 
• 35699-45-7 1-Methyl-2-naphthaldehyde 
• 35699-44-6 2-methyl-1-naphthaldehyde 
• 102606-06-4 Acetic acid 2-methyl-naphthalen-1-ylmethyl ester 
• 1575-96-8 2-methyl-1-naphthoic acid 
• 74661-65-7 1,11-Dimethyl-9,10-dioxa-tricyclo[6.2.2.0^2,7]dodeca-2⁽⁷⁾,3,5,11-tetraene 
• 126558-71-2 (2-Methyl-naphthalen-1-yl)-methyl-hydroperoxide 
• 2088-87-1 naphthalene-1,2-dicarboxylic acid 
• 33828-50-1 C₂₆H₂₂ 
• 20027-77-4 5,6-dimethyl-1,2,3,4-tetrahydronaphthalene 
• 36736-25-1 1,2-dimethyl-1,2,3,4-tetrahydronaphthalene 

Relevant articles and documents

Sterically hindered N-heterocyclic carbene/palladium(ii) catalyzed Suzuki-Miyaura coupling of nitrobenzenes

Palladium-catalyzed denitrative Suzuki coupling of nitroarenes using 2-aryl-5-(2,4,6-triisopropylphenyl)-2,3-imidazolylidene[1,5-a]pyridines as the ligands is described. The key to success is the use of the NHC ligands which show strong donating ability and suitable steric hindrance allowing the successful oxidative addition of Ar-NO2 bonds. Both aromatic and aliphatic boronic acids are tolerated, and a variety of biphenyls and alkylarenes were obtained in good to excellent yields.

Ni-Catalyzed cross-coupling of aryl thioethers with alkyl Grignard reagents via C-S bond cleavage

A Ni-catalyzed cross-coupling of aryl thioethers with alkyl Grignard reagents, accompanied by the cleavage of the C(aryl)-SMe bond, has been presented. This method is distinguished by its mild conditions and moderate functional group tolerance, such as hydroxyl, halogen, and heterocycles, which should provide a straightforward access to the modification of sulfur-containing molecules.

Methylation of naphthalene on MTW-type zeolites. Influence of template origin and substitution of Al by Ga

Two templates, methyltriethylammonium bromide (MTEA) and tetraethylammonium bromide (TEA) were used to synthesize aluminosilicate ZSM-12 zeolites. Additionally, zeolites isomorphously substituted (partially or totally) by gallium were prepared with MTEA.