16897-57-7

Basic information

• Product Name: 1,2,2a,3,4,5-hexahydroacenaphthylen-1-ol
• CAS NO: 16897-57-7
• Molecular Formula: C₁₂H₁₄O
• Molecular Weight: 174.239
• Mol File: 16897-57-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 319.3°C at 760 mmHg
• Flash Point: 117.1°C
• Density: 1.183g/cm³
• Vapor Pressure: 0.000142mmHg at 25°C
• Refractive Index: 1.625
• CAS DataBase Reference: 1,2,2a,3,4,5-hexahydroacenaphthylen-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,2a,3,4,5-hexahydroacenaphthylen-1-ol(16897-57-7)
• EPA Substance Registry System: 1,2,2a,3,4,5-hexahydroacenaphthylen-1-ol(16897-57-7)

Safety Data

• Hazardous Substances Data: 16897-57-7(Hazardous Substances Data)

Usage

General Description

1,2,2a,3,4,5-hexahydroacenaphthylen-1-ol is a chemical compound with the molecular formula C12H18O. It is a colorless liquid that is used primarily as a fragrance ingredient. 1,2,2a,3,4,5-hexahydroacenaphthylen-1-ol is a member of the acenaphthylene family and is classified as a cyclic alcohol. It is often used in the manufacturing of perfumes and other scented products due to its pleasant odor. Additionally, it has been studied for its potential pharmaceutical applications, including its antibacterial and antifungal properties. Overall, 1,2,2a,3,4,5-hexahydroacenaphthylen-1-ol is an important chemical in the fragrance and pharmaceutical industries due to its unique properties.

Upstream product

• 63328-18-7 3,4,5,10-tetrahydroacenaphthene-1-one 
• 63328-19-8 (1,2,3,4-tetrahydro-[1]naphthyl)-malonic acid diethyl ester 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 79781-33-2 1,2,3,4-tetrahydronaphthalene-1-acetic acid methyl ester 
• 79781-34-3 1,2,3,4-tetrahydronaphthalene-1-acetic acid chloride 
• 63328-17-6 2-(1,2,3,4-tetrahydronaphthalen-1-yl)acetic acid 
• 17516-09-5 1-carboxy-1,2,3,4-tetrahydronaphthalene-1-acetic acid 
• 74247-18-0 ethyl 2-cyano-2-(3,4-dihydronaphthalen-1(2H)-ylidene)acetate 
• 66258-75-1 1-carboxy-1,2,3,4-tetrahydronaphthalene-1-acetic acid anhydride 

Downstream Products

• 83-32-9 acenaphthene 
• 16897-56-6 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline 
• 951152-20-8 3,4-Trimethylen-inden 

Relevant articles and documents

BENZIMIDAZOLE COMPOUND AND PHARMACEUTICAL USE THEREOF

Provided is an ORL-1 receptor agonist having improved bioavailability based on superior metabolic stability and strong and high selectivity, as compared to conventional compounds. A compound represented by the formula (I) wherein each symbol is as defined

Abnormal Behaviour of Anhydrides of 1-Carboxy-1,2,3,4-tetrahydronaphthalene-1-acetic Acid and Its 7-Methyl Derivative in Presence of Anhydrous Aluminium Chloride: Synthesis of Acenaphthene and 3-Methylacenaphthene

Friedel-Crafts reaction of the anhydride of 1-carboxy-1,2,3,4-tetrahydronaphthalene-1-acetic acid (1a, R=H ) with benzene or toluene at 50-60 deg C affords 1,2,3,4-tetrahydronaphthalene-1-acetic acid (2a) and 10-carboxy-3,4,5,10-tetrahydroacenaphthene-1-one (3c).The anhydride of 1b (R=Me) similarly yields 7-methyl-1,2,3,4-tetrahydronaphthalene-1-acetic acid (2b). 2a,2b and their methyl esters have been converted into 3,4,5,10-tetrahydroacenaphthene-1-one (3a) and the 8-methyl analogue (3b) respectively. 3a and 3b on reduction afford 4a and 4b, which on dehydrogenation with Pd/C afford acenaphthene and 3-methylacenaphthene respectively. 3-Methylacenaphthene has also been synthesised by an alternate route starting from 7-methyltetralone.