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5α-Fern-8-ene is a naturally occurring chemical compound belonging to the class of steroids, specifically a fernane-type triterpene. It is characterized by a unique carbon skeleton with a five-membered ring at the A/B junction and an eight-membered ring at the C/D junction. 5α-Fern-8-ene is found in various plant species and has been studied for its potential biological activities, such as anti-inflammatory and anticancer properties. The structure of 5α-Fern-8-ene is defined by its specific arrangement of carbon atoms and functional groups, which contribute to its chemical properties and potential applications in pharmaceutical research.

1750-35-2

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1750-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1750-35-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1750-35:
(6*1)+(5*7)+(4*5)+(3*0)+(2*3)+(1*5)=72
72 % 10 = 2
So 1750-35-2 is a valid CAS Registry Number.

1750-35-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name fern-8-ene

1.2 Other means of identification

Product number -
Other names Isofernen

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1750-35-2 SDS

1750-35-2Relevant academic research and scientific papers

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

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