1,4-DIMETHYLNAPHTHALENE

1,4-DIMETHYLNAPHTHALENE Basic information
Product Name:1,4-DIMETHYLNAPHTHALENE
Synonyms:1,4-Dimethylnapthalene;naphthalene,1,4-dimethyl-;1,4-DIMETHYLNAPHTHALENE;1,4-DIMETHYLNAPHTHALENE 95+%;1,4-DIMETHYLNAPHTHALENE OEKANAL;1 4-DIMETHYLNAPHTHALENE OEKANAL 250 MG;1,4-Dimethylnaphthalene,~99%;1.4-Dimethylnaphthalene 100mg [571-58-4]
CAS:571-58-4
MF:C12H12
MW:156.22
EINECS:209-335-9
Product Categories:Bioactive Small Molecules;Building Blocks;Cell Biology;Chemical Synthesis;DIG-DY;Organic Building Blocks;Alpha Sort;Analytical Standards;AromaticsVolatiles/ Semivolatiles;Chemical Class;D;Arenes;Building Blocks;Organic Building Blocks;Naphthalene derivatives;DAlphabetic;DID - DINAnalytical Standards;Hydrocarbons;NaphthalenesChemical Class;NeatsAnalytical Standards;PAHsMore...Close...
Mol File:571-58-4.mol
1,4-DIMETHYLNAPHTHALENE Structure
1,4-DIMETHYLNAPHTHALENE Chemical Properties
Melting point -18 °C (lit.)
Boiling point 262-264 °C/751 mmHg (lit.)
density 1.016 g/mL at 25 °C (lit.)
refractive index n20/D 1.613(lit.)
Fp >230 °F
form neat
color Colorless to Light yellow to Light orange
Water Solubility 9.634mg/L(25 ºC)
BRN 2039842
LogP4.370
CAS DataBase Reference571-58-4(CAS DataBase Reference)
EPA Substance Registry System1,4-Dimethylnaphthalene (571-58-4)
Safety Information
Safety Statements 23-24/25
WGK Germany 3
RTECS QJ4440000
HS Code 2902.90.9000
MSDS Information
ProviderLanguage
SigmaAldrich English
1,4-DIMETHYLNAPHTHALENE Usage And Synthesis
Uses1,4-Dimethylnaphthalene is a polycyclic aromatic hydrocarbon (PAH) that has been found in dust particulate matter and is associated with activation of aryl hydrocarbon receptor as a major toxic mode of action in WB-F344 cell line. 1,4-Dimethylnaphthalene has been found to retard the development of epidermoid carcinomas in hamster buccal pouch. 1,4-Dimethylnaphthalene alters the genes associated with the maintenance of a G1/S phase block possibly through the induction of the cell cycle inhibitors KRP1 and KRP2 in potatoes.
DefinitionChEBI: A dimethylnaphthalene carrying methyl groups at positions 1 and 4.
Synthesis Reference(s)The Journal of Organic Chemistry, 46, p. 1251, 1981 DOI: 10.1021/jo00320a005
1,4-DIMETHYLNAPHTHALENE Preparation Products And Raw materials
Preparation Products1,4-Naphthalenedicarboxylic acid-->2,3-DIMETHYLNAPHTHALENE-->Naphthalene-->1,4-BIS(BROMOMETHYL)NAPHTHALENE
1,4,5,8-Naphthalenetetracarboxylic dianhydride 9,10-dibenzylanthracene 1,8-Dichloro-9,10-bis(phenylethynyl) anthracene Hypericin GOSSYPOL 9,10-DIMETHYLANTHRACENE 1-Chloro-9,10-bis(phenylethynyl)anthracene 10-METHYLANTHRACENE-9-CARBOXALDEHYDE 9,10-Diphenylanthracene 9,10-BIS(4-METHOXYPHENYL)ANTHRACENE 1,2,3,6,7,8-HEXAHYDROPYRENE 1,2,3,6,7,8,11,12-OCTAHYDROBENZO[E]PYREN-9(10H)-ONE 9,10-Di(2-naphthyl)anthracene 9,10-Bis(phenylethynyl)anthracene (3,3'-BI-7H-BENZ(DE)ANTHRACENE)-7,7'-DIONE 9,10-ANTHRACENEDICARBOXALDEHYDE 10-fluoro-7,12-dimethylbenz(a)anthracene 2-CHLORO-9,10-DIPHENYLANTHRACENE

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