54274-73-6 Usage
Description
(R)-1-Isopropyl-4-methyl-7-methylene-1,2,3,4,4a,5,6,7-octahydro-naphthalene, a bicyclic hydrocarbon with the molecular formula C15H24, is a colorless liquid characterized by its strong, aromatic odor. It is classified as a terpene, a group of organic compounds derived from plants with diverse biological and pharmacological properties.
Uses
Used in Fragrance Industry:
(R)-1-Isopropyl-4-methyl-7-methylene-1,2,3,4,4a,5,6,7-octahydro-naphthalene is used as a fragrance ingredient for its pleasant, woody scent, contributing to the creation of perfumes and personal care products.
Used in Essential Oils:
(R)-1-Isopropyl-4-methyl-7-methylene-1,2,3,4,4a,5,6,7-octahydro-naphthalene is also found in various essential oils, enhancing their aromatic qualities and providing a woody scent that is valued in the essential oil industry.
Used in Pharmaceutical Synthesis:
(R)-1-Isopropyl-4-methyl-7-methylene-1,2,3,4,4a,5,6,7-octahydro-naphthalene serves as a key component in the synthesis of various pharmaceuticals, leveraging its chemical properties to produce medicinal compounds.
Used as a Precursor in Organic Chemistry:
It acts as a precursor for the production of other organic compounds, indicating its versatility and importance in the field of organic chemistry for creating a range of useful substances.
Check Digit Verification of cas no
The CAS Registry Mumber 54274-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,7 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54274-73:
(7*5)+(6*4)+(5*2)+(4*7)+(3*4)+(2*7)+(1*3)=126
126 % 10 = 6
So 54274-73-6 is a valid CAS Registry Number.
54274-73-6Relevant articles and documents
STABLE CARBOCATIONS FROM TERPENOIDS. I. GENERATION OF CARBOCATIONS FROM NATURAL SESQUITERPENES - DERIVATIVES OF HEXAHYDRONAPHTHALENE
Osadchii, S. A.,Polovinka, M. P.,Korchagina, D. V.,Pankrushina, N. A.,Dubovenko, Zh. V.,et al.
, p. 1070 - 1081 (2007/10/02)
Stable enantio- and diastereomeric carbocations were generated for the first time from optically active sesquiterpenes (-)-α- and (-)-γ-murolenes (I) and (II) and (+)-γ- and (+)-δ-cadinenes (III) and (IV), and their rearrangements in media with various acidities were studied at tempetatures between -120 and 20 deg C.By the reaction of solutions of salts of the stable cations with nucleophiles the transition was realized from unconjugated dienes (I-IV), isolated from the resin of Pinus silvestris L., to the conjugated dienes (-)-zonarene (V), (-)- and (+)-10-epizonarenes (VI, VII), (-)-trans-isocadinene (VIII), and (-)-bicyclosesquiphellandrene (IX), which had been discovered previously in other plant sources.
