33214-70-9

Basic information

• Product Name: 1,2,3,4-tetrahydro-5-Methoxy-1,1-diMethylnaphthalene
• Synonyms: 1,2,3,4-tetrahydro-5-Methoxy-1,1-diMethylnaphthalene;5-Methoxy-1,1-diMethyl-1,2,3,4-tetrahydronaphthalene
• CAS NO: 33214-70-9
• Molecular Formula: C13H18O
• Molecular Weight: 190.28142
• EINECS: -0
• Mol File: 33214-70-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 277.5°Cat760mmHg
• Flash Point: 106.1°C
• Appearance: /
• Density: 0.957g/cm³
• Vapor Pressure: 0.0076mmHg at 25°C
• Refractive Index: 1.506
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1,2,3,4-tetrahydro-5-Methoxy-1,1-diMethylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-tetrahydro-5-Methoxy-1,1-diMethylnaphthalene(33214-70-9)
• EPA Substance Registry System: 1,2,3,4-tetrahydro-5-Methoxy-1,1-diMethylnaphthalene(33214-70-9)

Safety Data

• Hazardous Substances Data: 33214-70-9(Hazardous Substances Data)

Usage

General Description

1,2,3,4-tetrahydro-5-Methoxy-1,1-diMethylnaphthalene is a chemical compound with the molecular formula C13H16O. It is a naphthalene derivative and is also known by the name Tetralin. It is used in the production of insecticides, as a solvent for resins and waxes, and as a component in the formulation of dyes and perfumes. Tetralin is also used as a hydrogenation catalyst in the chemical industry. It is a colorless liquid with a mild odor and is considered to be relatively stable under normal conditions. However, it may be harmful if inhaled or ingested, and can cause irritation to the skin and eyes.

InChI:InChI=1/C13H18O/c1-13(2)9-5-6-10-11(13)7-4-8-12(10)14-3/h4,7-8H,5-6,9H2,1-3H3

Upstream product

• 2270-59-9 1-bromo-4-methylpent-3-ene 
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• 100-66-3 methoxybenzene 
• 171979-70-7 1-methoxy-2-(4-methylpent-3-en-1-yl)benzene 
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Downstream Products

• 109664-02-0 5,6,7,8-tetrahydro-3-hydroxy-2-[(1R)-2-hydroxy-1-methylethyl]-8,8-dimethyl-1,4-phenanthrenedione 
• 35825-57-1 Cryptotanshinone 
• 568-72-9 tanshinone-IIA 

Relevant articles and documents

Antitumor agents 269. Non-aromatic ring-A neotanshinlactone analog, TNO, as a new class of potent antitumor agents

Tetrahydroneotanshinlactone (TNT) and tetrahydronaphthalene-1-ol (TNO) derivatives were designed, synthesized, and evaluated for cytotoxic activity. The TNO derivatives were found to be a promising novel class of in vitro antitumor agents. The cyclohexene

Atomatic Annulation Strategy for the Synthesis of Angularly-Fused Diterpenoid Quinones. Total Synthesis of (+)-Neocryptotanshinone, (-)-Cryptotanshinone, Tanshinone IIA, and (+/-)-Royleanone

The application of a photochemical aromatic annulation strategy in highly efficient total syntheses of several diterpenoid quinones isolated from the traditional Chinese medicine Dan Chen is reported.The pivotal step in each synthesis involves the assembly of the key tricyclic intermediate via the application of a recently developed "second generation" photochemical aromatic annulation method for the construction of highly substituted aromatic systems.In the total synthesis of neocryptotanchinone, the synthesis of the requisite diazo ketone anulation substrate 7 was achieved using paladium-mediated coupling reactions and an intramolecular Friedel-Crafts cyclization to form key carbon-carbon bonds.The pivotal aromatic annulation reaction was then accomplished by irradiating a solution of the diazo ketone 7 and the readily availabe siloxyalkyne 6 in benzene at room temperature.The desired tricyclic phenol 16 was produced in 58-65percent yield and was then converted to (+)-neocryptotanshinone (1) by treatment with tetra-n-butylammonium fluoride in the presence of oxygen.Cyclization to generate (-)-cryptotanshinone (2) was accomplished in high yield by brief exposure of 1 to an ethanolic solution of concentrated sulfuric acid, and dehydrogenation of 2 with DDQ furnished tanshinone IIA (3).As a further demonstration of the utility of the photochemical aromatic annulation strategy in the construction of angularly-fused diterpenes, the total synthesis of (+/-)-royleanone (4) was also investigated.Irradiation of a solution of the diazo ketone 18 and siloxyalkyne 25 produced the tricyclic intermediate 26, which was converted in two steps to royleanone by desilylation and oxidation.