32885-82-8

Basic information

• Product Name: De-O-Methyllasiodiplodin
• Synonyms: De-O-Methyllasiodiplodin
• CAS NO: 32885-82-8
• Molecular Formula: C₁₆H₂₂O₄
• Molecular Weight: 278.34348
• Mol File: 32885-82-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 120-125℃ (hexane )
• Appearance: /
• CAS DataBase Reference: De-O-Methyllasiodiplodin(CAS DataBase Reference)
• NIST Chemistry Reference: De-O-Methyllasiodiplodin(32885-82-8)
• EPA Substance Registry System: De-O-Methyllasiodiplodin(32885-82-8)

Safety Data

• Hazardous Substances Data: 32885-82-8(Hazardous Substances Data)

Usage

General Description

De-O-Methyllasiodiplodin is a biological compound that is extracted from the fungus Botryosphaeria rhodina. Its chemical composition includes hydroxy groups, and it features a specific molecular weight. Scientists have been extensively studying this particular compound for potential medical applications. Studies suggest that it exhibits potent biological properties that can be used for developing potentially effective drugs to combat various diseases. However, there aren't many resources available with detailed information about this chemical compound.

Upstream product

• 125520-75-4 (R)-14-hydroxy-12-methoxy-3-methyl-3,4,5,6,7,8,9,10-octahydro-1H-benzo[c][1]oxacyclododecin-1-one 
• 502-42-1 cycloheptanone 
• 130877-77-9 (+)(R,S) methyl 2,4-dimethoxy-6-<8-hydroxy-9-(p-tolylsulfinyl) nonyl> benzoate 
• 130877-76-8 methyl 2,4-dimethoxy-6-(p-tolylsulfinyl) methyl benzoate 
• 130877-75-7 methyl 2,4-dimethoxy-6-<1-(p-tolylsulfonyl)-7-methoxycarbonyl heptyl> benzoate 
• 130877-72-4 (+)(R) methyl 3,5-dimethoxy-6-<8-oxo-9-(p-tolylsulfinyl) nonyl> benzoate 
• 130877-74-6 methyl 2,4-dimethoxy-6-(p-tolylsulfonyl) methyl benzoate 
• 130877-73-5 methyl 2,4-dimethoxy-6-(7-methoxycarbonyl) heptyl benzoate 
• 125520-73-2 (-)(R) 2,4-dimethoxy-6-(8-hydroxynonyl) benzoic acid 
• 125520-74-3 (R)-6-(8'-Hydroxynonyl)-2,4-dimethoxybenzoesaeure-methylester 
• 3686-57-5 2,4-dimethoxy-6-methylbenzoic acid 
• 7149-90-8 2,4-dimethoxy-6-methyl-benzaldehyde 
• 14565-11-8 methyl 7-hydroxyheptanoate 
• 38315-25-2 methyl 7-iodoheptanoate 

Downstream Products

• 1276020-06-4 C₂₃H₂₈O₄ 
• 1276020-13-3 C₃₀H₃₀O₆ 
• 1276020-17-7 C₃₀H₂₈Cl₂O₆ 
• 1276020-19-9 C₃₀H₃₄O₈S₂ 
• 1276020-15-5 C₃₀H₂₈Br₂O₆ 
• 1276020-08-6 C₃₀H₃₂N₂O₈ 

Relevant articles and documents

A Short and Efficient Approach for the Total Synthesis of (S)-Zearalenone and (R)-De-O-methyllasiodiplodin by Using Stille and RCM Protocols

A concise, flexible, and linear approach has been devised for the total synthesis of the resorcinylic acid lactones (S)-zearalenone (2) and (R)-de-O-methyllasiodiplodin (4) by using a Stille cross-coupling strategy. The other key steps of the synthesis include a ring-closing metathesis (RCM), a chemoselective reduction of an α,β-unsaturated ketone, and a transesterification reaction.

Asymmetric synthesis of orsellinic acid type macrolides: The example of lasiodiplodin

The asymmetric synthesis of both enantiomers of methyl lasiodiplodin is described. The chiral centers were created in the very last steps of the synthesis by asymmetric induction of a chiral sulfoxide group.