42719-34-6 Usage
Type of compound
Sesquiterpene alcohol
Explanation
A sesquiterpene is a type of terpene, which are organic compounds derived from isoprene units. Sesquiterpenes have three isoprene units and are commonly found in plants and fungi. The alcohol part indicates the presence of a hydroxyl (OH) group in the molecule.
Explanation
Aristolochene is the common name for this specific sesquiterpene alcohol, derived from its chemical structure and properties.
Explanation
Aristolochene is a naturally occurring compound that can be found in various plants and fungi, contributing to their unique scents and properties.
Explanation
Due to its appealing scent, aristolochene is often used in the production of fragrances and flavors, adding a distinct and pleasant aroma to various products.
Explanation
Research is being conducted on aristolochene to explore its potential as a medicinal compound, specifically for its possible antifungal and antibacterial properties.
Explanation
Aristolochene has been found to have insect repellent properties, making it a useful component in some insect control products to help keep insects at bay.
Explanation
The name of the compound indicates specific structural features, such as the presence of eight methyl (CH3) groups, two methylene (CH2) groups, and a docosatriene (a 22-carbon chain with three double bonds) backbone.
Explanation
Aristolochene is considered a complex chemical compound due to its large molecular size, numerous carbon and hydrogen atoms, and the presence of various functional groups and structural features.
Explanation
Aristolochene has a wide range of applications, including the production of fragrances and flavors, potential use in the development of new medicines, and as an active ingredient in insect control products.
Natural occurrence
Found in plants and fungi
Use in fragrances and flavors
Pleasant and aromatic scent
Medicinal properties
Potential antifungal and antibacterial activities
Insect repellent properties
Used in insect control products
Structural features
Octamethyl, bis(methylene), and docosatriene
Chemical complexity
Complex chemical compound
Applications
Fragrances, flavors, medicinal, and insect control
Check Digit Verification of cas no
The CAS Registry Mumber 42719-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,7,1 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42719-34:
(7*4)+(6*2)+(5*7)+(4*1)+(3*9)+(2*3)+(1*4)=116
116 % 10 = 6
So 42719-34-6 is a valid CAS Registry Number.
42719-34-6Relevant articles and documents
BIOSYNTHESIS OF UNUSUAL ACYCLIC ISOPRENOIDS IN THE ALGA BOTRYOCOCCUS BRAUNII
Wolf, Fred R.,Nemethy, Esther K.,Blanding, Jonathan H.,Bassham, James A.
, p. 733 - 738 (2007/10/02)
A 'resting state' isolate of the hydrocarbon-producing alga Botryococcus braunii photoassimilated sodium 14C>bicarbonate at rates comparable to fast growing algae, such as Chlorella ( > 150 μg atoms 14C/mg chlorophyll hr).Early in the reaction (up to several min), most of the radioactivity was associated with water-soluble metabolites.However, labeling of hexane-soluble compounds steadily increased from ca 3 percent at 15 sec to over 50 percent of the total incorporated 14C at 60 min.The purified hexane fraction, which consisted of a series of botryococcenes and squalene, constituted a relatively constant proportion (40-45percent) of the total hexane-soluble radioactivity at all bur the earliest time points ( a C30 botryococcene (ca 91 percent) and squalene (ca 8 percent); however, small amounts of radioactivity sequentially appeared in the C31, C32 and C34 botryococcenes.The results of pulse-chase experiments implicated the C30 botryococcene as the precursor of the higher homologues; during the chase, loss of radioactivity from the C30 compound was accompanied by a concomitant increase in the labelling of the C31 and C32 compounds.This study provides further evidence that the relatively slow growth of Botryococcus in culture may result, in part, from the diversion of a large proportion of reduced carbon into energetically expensive compounds and that the slower growth rate in the 'resting state' cannot be totally attributed to an impaired or intrinsically slow metabolism. - Key Wor Index - Botryococcus braunii; Chlorophyceae; alga; biosynthesis acyclic isoprenoids; botryococcenes.
