34169-69-2

Basic information

• Product Name: Pterosin Z
• Synonyms: Pterosin Z;2,3-Dihydro-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-1H-inden-1-one;Hypolepin B
• CAS NO: 34169-69-2
• Molecular Formula: C15H20O2
• Molecular Weight: 232.3181
• Mol File: 34169-69-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 394.2°Cat760mmHg
• Flash Point: 168.4°C
• Appearance: /
• Density: 1.074g/cm³
• Vapor Pressure: 6.37E-07mmHg at 25°C
• Refractive Index: 1.547
• CAS DataBase Reference: Pterosin Z(CAS DataBase Reference)
• NIST Chemistry Reference: Pterosin Z(34169-69-2)
• EPA Substance Registry System: Pterosin Z(34169-69-2)

Safety Data

• Hazardous Substances Data: 34169-69-2(Hazardous Substances Data)

Usage

General Description

Pterosin Z is a naturally occurring compound in the class of organic compounds known as pterosins. Pterosins are found in some species of ferns and are usually characterized by a highly substituted cyclopenta[c]pyran skeleton. Pterosin Z, like other pterosins, is primarily recognized for its biological activities. Although the specific properties and functions of Pterosin Z are not widely studied, pterosins typically exhibit various biological effects, including anticancer, antimicrobial, and antioxidant activities. The chemical characteristics and potential health benefits of Pterosin Z could pave the way for future research in pharmacology.

InChI:InChI=1/C15H20O2/c1-9-7-11-8-15(3,4)14(17)13(11)10(2)12(9)5-6-16/h7,16H,5-6,8H2,1-4H3

Upstream product

• 67-56-1 methanol 
• 127115-99-5 2,2,5-trimethyl-2'(H)-5',6'-dihydropyrano<3',4'-q> indan-1-one 
• 127115-97-3 2,2,5-trimethyl-2'(H)-5',6'-dihydropyrano<3',4'-q> indan-1-ol 
• 35944-01-5 6-<2-methoxyethyl>-2,2,5,7-tetramethylindan-1-one 
• 34175-96-7 2(R)-pterosin B 
• 74-88-4 methyl iodide 
• 17197-84-1 5,5-dimethylcyclopent-2-enone 
• 39482-46-7 2,2-dimethylpent-4-enoyl chloride 
• 16386-93-9 2,2-dimethylpent-4-enoic acid 
• 127116-00-1 7-bromomethyl-6-(2'-hydroxyethyl)-2,2,5-trimethylindan-1-one 

Relevant articles and documents

Ptaquiloside Z, a new toxic unstable sesquiterpene glucoside from the neotropical bracken fern Pteridium aquilinum var. caudatum

Reversed-phase HPLC fractionation, monitored by brine shrimp bioassay, led to the isolation of a new illudane-type sesquiterpene glucoside, ptaquiloside Z (2), as well as the known bracken carcinogen ptaquiloside (1), from a bioactive aqueous extract of the neotropical bracken fern Pteridium aquilinum var. caudatum (Pteridaceae). The structure of ptaquiloside Z (2) was confirmed by spectroscopic analyses and chemical degradation. Both compounds exhibited similar toxicity (LC50 62.5μg/ml at 24h and LC50 7.8μg/ml at 48h) toward brine shrimp. Copyright (C) 1997 Elsevier Science Ltd.

RHODIUM CATALYSED SYNTHESIS OF ILLUDALANES

A short, regiospecific route to pterosin Z and calomelanolactone is presented in which the key step is a rhodium catalysed intramolecular cycloaddition.

Synthesis and antispasmodic activity of nature identical substituted indanes and analogues

The synthesis of a series of substituted indanes which provide routes to nature-identical compounds and their analogues is reported. The smooth muscle relaxant activity of a series of substituted indanes and indanones together with their analogues has been measured. A compound with significant smooth muscle relaxant activity has been identified.