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.
Check Digit Verification of cas no
The CAS Registry Mumber 23747-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,4 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23747-14:
(7*2)+(6*3)+(5*7)+(4*4)+(3*7)+(2*1)+(1*4)=110
110 % 10 = 0
So 23747-14-0 is a valid CAS Registry Number.
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
23747-14-0Relevant articles and documents
Facile Synthesis of (=/-)-Isolongifolene and (+/-)-Isolongifolenedione Involving Ar1-5 Cyclisations
Ghosal, Manuka,Karpha, Tapan Kr.,Pal, Subrata Kr.,Mukherjee, Debabrata
, p. 2527 - 2528 (1995)
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
Robles-Dutenhefner, Patricia A.,da Silva Rocha, Kelly A.,Sousa, Edesia M.B.,Gusevskaya, Elena V.
experimental part, p. 72 - 79 (2009/09/25)
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
Das, Swati,Karpha, Tapan Kr.,Ghosal, Manuka,Mukherjee, Debabrata
, p. 1229 - 1232 (2007/10/02)
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.
