150256-11-4

Basic information

• Product Name: 2-Chloro-7-methylnaphthalene
• Synonyms: 2-Chloro-7-methylnaphthalene
• CAS NO: 150256-11-4
• Molecular Formula: C₁₁H₉Cl
• Molecular Weight: 176.64216
• Mol File: 150256-11-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 280.0±9.0 °C(Predicted)
• Appearance: /
• Density: 1.163±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Chloro-7-methylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Chloro-7-methylnaphthalene(150256-11-4)
• EPA Substance Registry System: 2-Chloro-7-methylnaphthalene(150256-11-4)

Safety Data

• Hazardous Substances Data: 150256-11-4(Hazardous Substances Data)

Upstream product

• 5436-21-5 acetylacetaldehyde dimethyl acetal 
• 55614-74-9 3-chlorobenzyl magnesium bromide 
• 1258788-70-3 trans-3-(p-chlorostyryl)furan 
• 498-60-2 furan-3-carboxaldehyde 
• 41904-39-6 3-chloro-benzeneacetyl chloride 
• 17556-19-3 7-chloro-3,4-dihydro-2(1H)-naphthalenone 
• 1878-65-5 3-chlorophenylacetic acid 

Relevant articles and documents

Construction of polyaromatics via photocyclization of 2-(fur-3-yl) ethenylarenes, using a 3-furyl group as an isopropenyl equivalent synthon

The construction of different types of substituted arenes was demonstrated through the photocyclization of 2-(fur-3-yl)ethenylarenes using a 3-furyl group as an isopropenyl equivalent synthon in the photocyclization reaction. The furan portion of the photocyclization intermediate could be fragmented via a base-induced elimination reaction to yield a series of substituted polyaromatics, including naphthalene, benzofuran, benzothiophene, phenanthrene, phenalene, acenaphthene, and triphenylene. Using different reagents, this method made it possible to introduce methyl or 2-hydroxyethyl groups as substituents at specific positions in these arenes.

Antihyperglycemic Activity of Novel Naphthalenyl 3H-1,2,3,5-Oxathiadiazole 2-Oxides

A series of naphthalenyl 3H-1,2,3,5-oxathiadiazole 2-oxides was prepared and tested for antihyperglycemic activity in the db/db mouse, a model for type 2 (non-insulin dependent) diabetes mellitus.Substitution at the 1-,5-, or 8-positions of the naphthalene ring with a halogen was found to be beneficial to antihyperglycemic activity. 4--3H-1,2,3,5-oxathiadiazole 2-oxide (45), one of the most potent compounds in this series, was selected for further pharmacological evaluation.