23747-14-0

Usage

Uses

Used in Fragrance Industry:
1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-7H-2,4a-methanonaphthalen-7-one is used as a base note in perfumes for its strong, sweet, musky scent, contributing to the long-lasting and rich aroma of fragrances.
Used in Flavor Industry:
In the flavor industry, 1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-7H-2,4a-methanonaphthalen-7-one is used to impart a distinctive, sweet, and musky taste to various food and beverage products, enhancing their overall flavor profile.
Used in Pharmaceutical Industry:
1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-7H-2,4a-methanonaphthalen-7-one may have applications in the pharmaceutical industry, potentially serving as an active ingredient or intermediate in the development of new drugs, leveraging its unique chemical properties.
Used in Chemical Industry:
In the chemical industry, 1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-7H-2,4a-methanonaphthalen-7-one could be utilized in the synthesis of various chemical products, taking advantage of its ketone and cyclic structures for further reactions and applications.

InChI:InChI=1/C15H22O/c1-13(2)9-11(16)7-12-14(3,4)10-5-6-15(12,13)8-10/h7,10H,5-6,8-9H2,1-4H3

Upstream product

• 15681-48-8 lithium dimethylcuprate 
• 72008-96-9 1,1,5-Trimethyl-1,2,3,4-tetrahydro-2,4a-methano-naphthalen-7-one 
• 17015-38-2 isolongifolene 
• 140869-28-9 (4-Methoxy-1,1-dimethyl-3-oxo-indan-2-yl)-acetic acid methyl ester 
• 140869-29-0 2-(4-Methoxy-1,1-dimethyl-indan-2-yl)-ethanol 
• 140869-30-3 2-(2-Bromo-ethyl)-4-methoxy-1,1-dimethyl-indan 
• 140869-25-6 2-(2-Bromo-ethyl)-1,1-dimethyl-indan-4-ol 
• 140869-31-4 1,1-Dimethyl-1,2,3,4,6,7-hexahydro-2,4a-methano-naphthalen-5-one 
• 140869-26-7 1,1-Dimethyl-1,2,3,4-tetrahydro-2,4a-methano-naphthalen-5-one 
• 140869-27-8 7-Methoxy-3,3-dimethyl-indan-1-one 
• 140869-32-5 1,1,5-Trimethyl-1,3,4,7-tetrahydro-2H-2,4a-methano-naphthalene 
• 81945-09-7 7-hydroxy-3,3-dimethyl-indan-1-one 
• 54897-52-8 phenyl 3,3-dimethylacrylate 
• 3350-78-5 3,3-Dimethylacryloyl chloride 

Relevant academic research and scientific papers

Facile Synthesis of (=/-)-Isolongifolene and (+/-)-Isolongifolenedione Involving Ar1-5 Cyclisations

Facile syntheses of (+/-)-isolongifolene 2 and (+/-)-isolongifolenedione 20 have been accomplished utilising aryl participated cyclisations of the bromophenol 15 and the diazoketone 11 respectively as the key steps.

Cobalt-catalyzed oxidation of terpenes: Co-MCM-41 as an efficient shape-selective heterogeneous catalyst for aerobic oxidation of isolongifolene under solvent-free conditions

Cobalt-containing MCM-41 was used as a heterogeneous catalyst for the liquid-phase aerobic oxidation of isolongifolene, one of the most available sesquiterpenes. The material was prepared by direct incorporation of cobalt into the framework through the hy

Aryl participated cyclisations involving indane derivatives a total synthesis of (±)-isolongifolene

A total synthesis of (±)-isolongifolene (1) has been accomplished using intramolecular anionic cyclisation of the bromophenol 2 as the key step. Aryl participated intramolecular cyclisation of the diamethyl ketones 17 and 23 provided the dienediones 18 and 24 which were stereoselectively converted into the diketones 19 and 25 respectively.