189264-45-7

Basic information

• Product Name: Cleroindicin D
• Synonyms: Cleroindicin D
• CAS NO: 189264-45-7
• Molecular Formula: C8H12O4
• Molecular Weight: 172.18
• Mol File: 189264-45-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cleroindicin D(CAS DataBase Reference)
• NIST Chemistry Reference: Cleroindicin D(189264-45-7)
• EPA Substance Registry System: Cleroindicin D(189264-45-7)

Safety Data

• Hazardous Substances Data: 189264-45-7(Hazardous Substances Data)

Usage

General Description

Cleroindicin D is a natural chemical compound isolated from the plants of the genus Clerodendrum. It belongs to the class of compounds known as diterpenoids and has shown various pharmacological activities, including anti-inflammatory, antioxidant, and antitumor properties. Studies have also demonstrated its potential in preventing neurodegenerative diseases and as an antibacterial agent. Cleroindicin D is an important molecule in the search for new pharmaceuticals and its biological activities make it a promising candidate for the development of drugs targeting various ailments.

Upstream product

• 1133797-39-3 C₂₃H₅₀O₈SSi₂ 
• 1159796-01-6 C₈H₁₀O₄ 

Downstream Products

• 189264-47-9 (3aR,7aR)-3a-hydroxy-3,3a,7,7a-tetrahydrobenzofuran-6(2H)-one 

Relevant articles and documents

Desymmetrization of cyclohexadienones via bronsted acid-catalyzed enantioselective oxo-michael reaction

Chemical Reaction Reprentation Desymmetrlzatlon of cyclohexadlenones via enantloselectlve oxo-Mlchael reaction catalyzed by chlral phosphoric add to afford highly enantloenrlched 1,4-dloxane and tetrahydrofuran derivatives In excellent yields has been realized. The newly established methodology allows the facile enantloselectlve synthesis of clerolndlclns C, D, and F.Copyright

Enantioselective total synthesis of all of the known chiral cleroindicins (C-F): Clarification among optical rotations and assignments

(Chemical Equation Presented) Enantioselective syntheses of all of the named chiral members of the cleroindicin family (C-F) are reported. This effort demonstrates the synthetic utility of a 2,4-dihydroxybenzaldehyde as a starting material for natural pro