41743-38-8

Basic information

• Product Name: Bavachromene
• Synonyms: Bavachromene;(2E)-1-(7-Hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-3-(4-hydroxyphenyl)-2-propene-1-one;(E)-1-(7-Hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-3-(4-hydroxyphenyl)-2-propen-1-one;(2E)-1-(7-Hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-3-(4-hydroxyphenyl)-2-propen-1-one;Psorachromene
• CAS NO: 41743-38-8
• Molecular Formula: C20H18O4
• Molecular Weight: 322.35
• Mol File: 41743-38-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Bavachromene(CAS DataBase Reference)
• NIST Chemistry Reference: Bavachromene(41743-38-8)
• EPA Substance Registry System: Bavachromene(41743-38-8)

Safety Data

• Hazardous Substances Data: 41743-38-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Bavachromene is used as a therapeutic agent for its anti-inflammatory properties, helping to reduce inflammation in various conditions.
Bavachromene is used as an anti-fungal agent, combating fungal infections due to its inherent anti-fungal activity.
Bavachromene is used as a neuroprotective agent, safeguarding the nervous system and potentially treating neurodegenerative diseases.
Used in Oncology:
Bavachromene is used as an anti-cancer agent, inhibiting the growth of cancer cells and offering a potential therapeutic option for cancer treatment.
Used in Drug Development:
Bavachromene is used as a lead compound in drug discovery, guiding the development of new medications that leverage its diverse therapeutic effects.

Upstream product

• 19013-03-7 6-acetyl-7-hydroxy-2,2-dimethyl-1H-chromene 
• 123-08-0 4-hydroxy-benzaldehyde 
• 28437-37-8 5-C-prenylresacetophenone 
• 74189-56-3 4-(tetrahydropyran-2-yloxy)benzaldehyde 

Relevant articles and documents

Natural product-like combinatorial libraries based on privileged structures. 1. General principles and solid-phase synthesis of benzopyrans

Herein we report a novel strategy for the design and construction of natural and natural product-like libraries based on the principle of privileged structures, a term originally introduced to describe structural motifs capable of interacting with a variety of unrelated molecular targets. The identification of such privileged structures in natural products is discussed, and subsequently the 2,2-dimethylbenzopyran moiety is selected as an inaugural template for the construction of natural product-like libraries via this strategy. Initially, a novel solid-phase synthesis of the benzopyran motif is developed employing a unique cycloloading strategy that relies on the use of a new, polystyrene-based selenenyl bromide resin. Once the loading, elaboration, and cleavage of these benzopyrans was established, this new solid-phase method was then thoroughly validated through the construction of six focused combinatorial libraries designed around natural and designed molecules of recent biological interest.

13C Nuclear Magnetic Resonance Studies on Pyrano- and Dihydropyrano-1,3-diphenylprop-2-enones

The 13C NMR spectra of 19 differently substituted pyrano- and dihydropyrano-1,3-diphenylprop-2-enones were recorded and the results are discussed.The data will be useful in the identification of new and natural chalcones. Key Words: Chalcones - 1,3-Diphen