30316-17-7

Basic information

• Product Name: 1,2,3,4-Tetrahydro-2,5,8-trimethylnaphthalene
• Synonyms: 1,2,3,4-Tetrahydro-2,5,8-trimethylnaphthalene;2,5,8-Trimethyltetralin;Naphthalene, 1,2,3,4-tetrahydro-2,5,8-trimethyl-
• CAS NO: 30316-17-7
• Molecular Formula: C₁₃H₁₈
• Molecular Weight: 174.282
• Mol File: 30316-17-7.mol
• Article Data: 1

Chemical Properties

• Melting Point: -7.5°C (estimate)
• Boiling Point: 265.28°C (estimate)
• Flash Point: 107.7°C
• Appearance: /
• Density: 0.9336 (estimate)
• Vapor Pressure: 0.0183mmHg at 25°C
• Refractive Index: 1.5216 (estimate)
• CAS DataBase Reference: 1,2,3,4-Tetrahydro-2,5,8-trimethylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-Tetrahydro-2,5,8-trimethylnaphthalene(30316-17-7)
• EPA Substance Registry System: 1,2,3,4-Tetrahydro-2,5,8-trimethylnaphthalene(30316-17-7)

Safety Data

• Hazardous Substances Data: 30316-17-7(Hazardous Substances Data)

Usage

Physical state

Liquid The compound exists in a liquid state at room temperature.

Color

Colorless The liquid is transparent and lacks any color.

Odor

Sweet, floral The compound has a pleasant, sweet scent reminiscent of flowers.

Usage in perfumes and cosmetics

Fragrance ingredient The compound is used to provide a pleasant scent in perfumes and other cosmetic products.

Usage in the food industry

Flavoring agent The compound is added to food products to enhance or modify their taste.

Application in synthetic musk production

Production of synthetic musk compounds The compound serves as a starting material or intermediate in the synthesis of musk-like compounds.

Use as a solvent

Solvent in chemical reactions The compound can dissolve other substances, making it useful as a solvent in various chemical processes.

Restricted use

Environmental and health concerns In some regions, the use of 1,2,3,4-Tetrahydro-2,5,8-trimethylnaphthalene has been limited due to potential negative impacts on the environment and human health.

InChI:InChI=1/C13H18/c1-9-4-7-12-10(2)5-6-11(3)13(12)8-9/h5-6,9H,4,7-8H2,1-3H3

Upstream product

• 16206-40-9 4-(2,5-dimethylphenyl)-2-methyl-4-oxobutanoic acid 
• 16206-39-6 3-(2.5-Dimethylbenzoyl)-buttersaeure 
• 30316-14-4 4-(2,5-dimethylphenyl)-2-methylbutanoic acid 
• 30275-76-4 4-(2,5-Dimethyl-phenyl)-3-methyl-butyric acid 
• 106-42-3 para-xylene 
• 160715-86-6 isopropyl (Z)-2-(diethoxyphosphinyl)-5,9-dimethyldeca-2,8-dienoate 
• 10468-59-4 2,5,8-trimethyl-3,4-dihydro-1(2H)-naphthalenone 
• 10468-60-7 3,5,8-trimethyl-3,4-dihydro-1(2H)-naphthalenone 

Downstream Products

• 2131-42-2 1,4,6-trimethylnaphthalene 

Relevant articles and documents

Intramolecular ene reaction of vinylphosphonates. Synthetic application to bicyclic compounds and cadalane and valerenic acid terpenoids

The Lewis-acid-catalyzed intramolecular ene reaction of vinylphosphonates 4, 6, and 7, prepared by the Knoevenagel condensation of triethyl phosphonoacetate (3) with citronellal (1) or 2,6-dimethyl-5-heptenal (2), stereoselectively gave 2-(8'-p-menthen-3'