131652-35-2

Usage

Uses

Used in Pharmaceutical Industry:
8-(1-Chloro-2-hydroxy-3-methylbut-3-enyl)-7-methoxycoumarin is used as a potential pharmaceutical agent for its possible anticoagulant, anti-inflammatory, and anticancer properties. The presence of various functional groups in its structure may enhance or modify these biological effects, making it a candidate for further research and development in drug discovery.
Used in Research and Development:
In the field of scientific research, 8-(1-Chloro-2-hydroxy-3-methylbut-3-enyl)-7-methoxycoumarin serves as a subject for investigation to explore its potential pharmacological properties and understand how the specific chemical modifications contribute to its biological activities. This research can lead to the discovery of new therapeutic agents or the enhancement of existing ones.

InChI:InChI=1/C15H15ClO4/c1-8(2)14(18)13(16)12-10(19-3)6-4-9-5-7-11(17)20-15(9)12/h4-7,13-14,18H,1H2,2-3H3

Upstream product

• 6545-99-9 phebalosin 

Related news

Formation and reduction of No (cas 131652-35-2) from the oxidation of NH3/CH4 with high concentration of H2O07/23/2019

This study investigated the homogeneous formation and reduction of NO from the oxidation of CH4/NH3 to understand the effect of the high concentrations of H2O on NO emissions. The experimental results about the effects of excess oxygen ratio, gas compositions including H2O, CO2, NH3 and recycled...detailed

No (cas 131652-35-2) trade and yes trade theorems for heterogeneous priors07/22/2019

We show that contrary to currently widely-held misperceptions, the classical no trade theorem obtains even under heterogeneous priors. That is, when priors are not common, speculative trade is still impossible under common knowledge of rationality. However, trade becomes mutually acceptable if a...detailed

Selective catalytic reduction of No (cas 131652-35-2) with CO and C3H6 over Rh/NbOPO407/21/2019

The selective catalytic reduction of NO with C3H6 and CO was investigated over platinum group metal (PGM; Pd, Rh, or Pt) supported on NbOPO4. Rh/NbOPO4 exhibits a lower light-off temperature of NO reduction to N2 compared to Pd- or Pt-loaded NbOPO4 catalysts and Rh/Al2O3 under stoichiometric con...detailed

Relevant academic research and scientific papers

The Chemical Composition of Murraya paniculata. The Structure of Five New Coumarins and One New Alkaloid and the Stereochemistry of Murrangatin and Related Coumarins

The structural determination of five new coumarins: murralonginol isovalerate (1b), isomurralonginol isovalerate (2b), murrangatin isovalerate (6b), minumicrolin isovalerate (7b), chlocucol (4a), and a new indole alkaloid, paniculol (18), is described.The relative configurations hitherto reported for the α-glycol moieties in murrangatin (erythro) and minumicrolin (threo) have been revised to threo for compound (6a) and erythro for compound (7a), respectively on the basis of NOE experiments performed on the acetonides (6e) and (7e).Furthermore, the absolute configuration of (-)-murrangatin (6a) has been shown to be by analysis of the CD spectrum of tetrahydromurrangatin dibenzoate (16b).The reaction of phebalosin (8) with hydrochloric acid has also been re-examined.