1615-99-2 Usage
Description
FERN-9(11)-ENE is a natural organic compound belonging to the class of diterpenes, which are hydrocarbons derived from the combination of two isoprene units. It is found in a variety of plants, including ferns, and is known for its potential biological activities such as anti-inflammatory, anti-fungal, and anti-cancer properties. Its chemical structure consists of a fused four-ring system with a characteristic double bond at the 9(11) position, giving it its unique and important chemical properties.
Used in Pharmaceutical Industry:
FERN-9(11)-ENE is used as a pharmaceutical agent for its potential anti-inflammatory, anti-fungal, and anti-cancer properties. Its biological activities make it a promising candidate for the development of new drugs to treat various diseases.
Used in Flavor and Fragrance Industry:
FERN-9(11)-ENE is used as a flavoring agent in food products due to its unique chemical properties. Its characteristic double bond at the 9(11) position contributes to its distinct aroma and flavor, making it a valuable ingredient in the creation of food products with specific taste profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 1615-99-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1615-99:
(6*1)+(5*6)+(4*1)+(3*5)+(2*9)+(1*9)=82
82 % 10 = 2
So 1615-99-2 is a valid CAS Registry Number.
InChI:InChI=1/C30H50/c1-20(2)21-10-13-25-28(21,6)18-19-29(7)23-11-12-24-26(3,4)15-9-16-27(24,5)22(23)14-17-30(25,29)8/h14,20-21,23-25H,9-13,15-19H2,1-8H3/t21-,23+,24+,25-,27-,28-,29-,30+/m1/s1
1615-99-2Relevant articles and documents
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Gonzalez,A.G. et al.
, p. 1547 - 1549 (1974)
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Spiro-triterpenes from clay-catalysed rearrangement of hopenes: NMR structural elucidation and occurrence in a recent sediment
Hauke,Hauke, Verena,Trendel,Trendel, Jean M.,Albrecht,Albrecht, Pierre,Connan,Connan, Jacques
, p. 2227 - 2230 (2007/10/02)
Acidic K-10 montmorillonite clay-catalysed rearrangement of hop-22(29)-ene 5 and of hop-17(21)-ene 6 leads to the formation of small quantities of various fernenes and of new compounds, the 14-methyl-13,15-cyclo-B':A'-neo-26-nor-14,15-seco-18α-gammacer-7-ene 8 and its Δ8- and Δ9((11))-isomers 9 and 10, the structures of which have been established by MS and NMR spectroscopy. This novel hopane skeleton transposition also operates on bacterial sedimentary hopenes, as shown by GC-MS investigations of the alkene fraction from a recent lacustrine sediment.
Acid-Induced Rearrangement of Triterpenoid Hydrocarbons Belonging to the Hopane and Migrated Hopane Series
Ageta, Hiroyuki,Shiojima, Kenji,Arai, Yoko
, p. 2705 - 2716 (2007/10/02)
The acid-catalyzed rearrangement of triterpenoid monoenes belonging to the hopane and migrated hopane series with sulfuric acid and boron trifluoride etherate was investigated.By selecting the reaction conditions, a variety of the monoenes of these series, including three new compounds, 9βH-fern-7-ene (3c), 8βH-fern-9(11)-ene (4b), and adian-5(10)-ene (5b), were obtained.For comparison, oleanenes and migrated oleanenes were also subjected to the same reaction.Keywords--acid-induced rearrangement; triterpenoid hydrocarbon; hopane, migrated hopane; 9βH-fern-7-ene; 8βH-fern-9(11)-ene; adian-5(10)-ene; sulfuric acid; boron trifluoride