23747-14-0 Usage
General Description
The chemical "1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-7H-2,4a-methanonaphthalen-7-one" is a synthetic compound with a complex molecular structure. It is a ketone, meaning it contains a carbonyl group attached to two alkyl groups. The compound also contains six carbon atoms arranged in a cyclic structure, with additional methyl groups attached to the carbon atoms. This chemical is commonly used in the production of fragrances and flavors due to its unique aromatic properties. It has a strong, sweet, musky scent and is often used as a base note in perfumes. Additionally, it may also have applications in the pharmaceutical and chemical industries.
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.
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.