121242-02-2

Basic information

• Product Name: KS IV
• Synonyms: KS IV
• CAS NO: 121242-02-2
• Molecular Formula: C₁₇H₁₂O₆
• Molecular Weight: 312.27358
• Mol File: 121242-02-2.mol

Chemical Properties

• Boiling Point: 629.7°Cat760mmHg
• Flash Point: 348.6°C
• Appearance: /
• Density: 1.6g/cm³
• Vapor Pressure: 1.01E-16mmHg at 25°C
• Refractive Index: 1.796
• CAS DataBase Reference: KS IV(CAS DataBase Reference)
• NIST Chemistry Reference: KS IV(121242-02-2)
• EPA Substance Registry System: KS IV(121242-02-2)

Safety Data

• Hazardous Substances Data: 121242-02-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H12O6/c18-13-2-1-8(5-14(13)19)11-4-10(17(22)23)3-9-6-15(20)16(21)7-12(9)11/h1-7,18-21H,(H,22,23)

Upstream product

• 110664-69-2 6,7-dimethoxy-4-(3,4-dimethoxyphenyl)naphthalene-2-carboxylic acid 
• 130508-46-2 Cannabisin A 
• 121242-03-3 methyl-6,7-dimethoxy-4-(3,4-dimethoxyphenyl)naphthalene-2-carboxylate 

Downstream Products

• 121242-03-3 methyl-6,7-dimethoxy-4-(3,4-dimethoxyphenyl)naphthalene-2-carboxylate 

Relevant articles and documents

9-norlignans: Occurrence, properties and their semisynthetic preparation from hydroxymatairesinol

Lignans, neolignans, norlignans and norneolignans constitute a large class of phenolic natural compounds. 9-Norlignans, here defined to contain a β-β' bond between the two phenylpropanoid units and to lack carbon number 9 from the parent lignan structure, are the most rarely occurring compounds within this class of natural compounds. We present here an overview of the structure, occurrence and biological activity of thirty-five 9-norlignans reported in the literature to date. In addition, we report the semisynthetic preparation of sixteen 9-norlignans using the natural lignan hydroxymatairesinol obtained from spruce knots, as starting material. 9-Norlignans are shown to exist in different species and to have various biological activities, and they may therefore serve as lead compounds for example for the development of anticancer agents. Hydroxymatairesinol is shown to be a readily available starting material for the preparation of norlignans of the imperanene, vitrofolal and noralashinol family.

Moose, eine Quelle biologisch aktiver Naturstoffe?

Die in chemischer Hinsicht lange vernachlaessigte Pflanzenabteilung der Moose (Bryophyta) erweist sich geradezu als Fundgrube fuer neue Naturstoffe einschliesslich solcher mit neuartigen Strukturtypen.Zahlreiche dieser Stoffe zeigen recht beachtliche biol

CANNABISIN A, AN ARYLNAPHTHALENE LIGNANAMIDE FROM FRUITS OF CANNABIS SATIVA

A new lignanamide, named cannabisin A, a known lignanamide, grossamide, and three known amides, N-trans-caffeoyltyramine, N-trans-feruloyltyramine, N-p-coumaroyltyramine, were isolated from the fruits of Cannabis sativa.The structure of cannabisin A has been established as 6,7-dihydroxy-1-(3,4-dihydroxyphenyl)-N1,N2-bis--2,3-naphthalenedicarboxamide, on the basis of chemical and spectral evidence.Key Word Index - Cannabis sativa; Cannabidaceae; fruits; cannabisin A; grossamide; N-trans-caffeoyltyramine; N-trans-feruloyltyramine; N-p-coumaroyltyramine.

ISOLATION AND SYNTHESIS OF 6,7-DIHYDROXY-4-(3,4-DIHYDROXYPHENYL)NAPHTHALENE-2-CARBOXYLIC ACID FROM PELLIA EPIPHYLLA

A new naphthalene derivative, 6,7-dihydroxy-4-(3,4-dihydroxyphenyl)naphthalene-2-carboxylic acid has been isolated from gametophytic tissues of the liverwort Pellia epiphylla.The structure of the compound was elucidated by means of spectroscopic methods a