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144506-19-4

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144506-19-4 Usage

General Description

Cannabisin D is a chemical compound found in cannabis plants that belongs to the group of cannabinoids. It is a dimeric form of the well-known cannabinoid, cannabidiol (CBD), and has been found to exhibit potential anti-inflammatory and anti-cancer properties. Research has shown that cannabisin D may have the ability to inhibit the growth of cancer cells and reduce inflammation in the body. It also possesses antioxidant properties and has shown promise in the treatment of neurodegenerative diseases. Furthermore, it has been reported to have minimal psychotropic effects, making it a potentially valuable therapeutic agent with a wide range of medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 144506-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,5,0 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144506-19:
(8*1)+(7*4)+(6*4)+(5*5)+(4*0)+(3*6)+(2*1)+(1*9)=114
114 % 10 = 4
So 144506-19-4 is a valid CAS Registry Number.

144506-19-4Downstream Products

144506-19-4Relevant articles and documents

Regioselective Oxidation Approaches to Concise Synthesis of (±)-Canabisin D

Li, Wenling,Liu, Qian,Liu, Hao,Chen, Peilan,Yang, Xi,Liu, Yingying

, p. 717 - 722 (2015/12/05)

The regioselective effects of tert-butyl or bromine as the position-protecting group of feruloytyamide on the oxidative coupling reactions for the synthesis of natural (±)-canabisin D were investigated in detail. The coupling yield of 8-8-coupled aryldihydronaphthalene product of 5-Br-feruloytyamide was higher than that of tert-butyl substituted precursor under FeCl3·6H2O-acetone-water oxidative condition. FeCl3·6H2O-catalyzed oxidative coupling reactions of feruloytyamide protected by tert-butyl or bromine group produced the desired 8-8-coupled aryldihydronaphthalene products, which underwent the debutylation or debromination to concisely synthesize (±)-canabisin D.

TERMITE ANTIFEEDANT ACTIVITY IN XYLOPIA AETHIOPICA

Lajide, Labunmi,Escoubas, Pierre,Mizutani, Junya

, p. 1105 - 1112 (2007/10/02)

A heaxne extract of xylopia aethiopica fruits and an aqueous methanol extract of the seeds were studied for termite antifeedant activity against workers of the subterranean termite, Reticullitermes speratus.The crude extract, at1percent exhibited strong antifeedant activity in a choice filter paper disk bioassay.Bioassay-directed fractionation led to the isolation and identification of six ent-kaurane diterpenes in the hexane extract.Feeding deterrent activity varied significantly with the structures when the compounds were tested at concentrations ranging from 5000 ppm (40 μg cm-2) to 100 ppm (0.824 μg cm-2). (-)-Kaur-16-en-19-oic acid had the strongest termite antifeedants activity among the ent-kauranes isolated.Two phenolic amides and four lignanamides were also isolated from the aqueous methanolic extract of seeds.E-3-(4-hydroxy-3-methoxyphenyl)-N-2-2-propenamide was more active than E-3 (3,4-dihydroxyphenyl)-N-2-2-propenamide, whilst grossamide and the new lignanamide, demethylgrossamide, as well as (-)-cannabisins B and D exhibited potent feeding deterrent activity at 5000 ppm.The identity of these compounds was established by spectroscopic analysis and synthesis.Two synthetic amides, E-3-(3,4-methylenedioxyphenyl)-N-2- propenamide and E-3-(3,4-methylenedioxyphenyl)-N-2--2-propenamide were also tested for antifeedant activity. - Keywords: xylopia aethiopica; Annonaceae; seeds; fruits; Reticullitermes speratus; Isoptera; antifeedants; ent-kaurane diterpenes; phenolic amides; lignanamides.

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