582-16-1 | 2,7-Dimethylnaphthalene

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$10.00	$7.00
1g	97%	in stock	$42.00	$29.00
10g	97%	in stock	$387.00	$271.00
100g	97%	in stock	$3,693.00	$2,585.00

Description

• Catalog Number: AB60751
• Chemical Name: 2,7-Dimethylnaphthalene
• CAS Number: 582-16-1
• Molecular Formula: C12H12
• Molecular Weight: 156.2237
• MDL Number: MFCD00004121
• SMILES: Cc1ccc2c(c1)cc(cc2)C
• NSC Number: 36851

Computed Properties

• Complexity: 134
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• XLogP3: 4.3

Upstream Synthesis Route

2,7-Dimethylnaphthalene is a versatile compound frequently employed in chemical synthesis for its unique properties. As a substituted naphthalene derivative, it serves as a valuable starting material for the creation of various organic compounds through a range of reactions. This compound is particularly useful in the production of functionalized naphthalene derivatives, which find applications in pharmaceuticals, agrochemicals, and materials science. Additionally, 2,7-Dimethylnaphthalene can act as a precursor in the synthesis of advanced materials such as liquid crystals, polymers, and dyes. Its role in chemical synthesis highlights its significance as a building block for the development of diverse compounds with tailored properties and functionalities.

Literature

• Effect of NO₂ concentration on dimethylnitronaphthalene yields and isomer distribution patterns from the gas-phase OH radical-initiated reactions of selected dimethylnaphthalenes.

  Environmental science & technology 20120717

• 3,8-Dimethyl-acenaphthyl-ene-1,2-dione.

  Acta crystallographica. Section E, Structure reports online 20110801

• Exploring QSAR and QAAR for inhibitors of cytochrome P450 2A6 and 2A5 enzymes using GFA and G/PLS techniques.

  European journal of medicinal chemistry 20090501

• Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors.

  Journal of medicinal chemistry 20050602

• Quantitative structure-activity relationship analysis of inhibitors of the nicotine metabolizing CYP2A6 enzyme.

  Journal of medicinal chemistry 20050127

• Anaerobic oxidation of crude oil hydrocarbons by the resident microorganisms of a contaminated anoxic aquifer.

  Environmental science & technology 20031115