79320-84-6

Basic information

• Product Name: (4alpha)-15-(acetyloxy)-3-oxo-12,13-epoxytrichothec-9-en-4-yl chloroacetate
• CAS NO: 79320-84-6
• Molecular Formula: C₁₉H₂₃ClO₇
• Molecular Weight: 398.8347
• Mol File: 79320-84-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 501.1°C at 760 mmHg
• Flash Point: 181.3°C
• Density: 1.38g/cm³
• Vapor Pressure: 3.59E-10mmHg at 25°C
• Refractive Index: 1.561
• CAS DataBase Reference: (4alpha)-15-(acetyloxy)-3-oxo-12,13-epoxytrichothec-9-en-4-yl chloroacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (4alpha)-15-(acetyloxy)-3-oxo-12,13-epoxytrichothec-9-en-4-yl chloroacetate(79320-84-6)
• EPA Substance Registry System: (4alpha)-15-(acetyloxy)-3-oxo-12,13-epoxytrichothec-9-en-4-yl chloroacetate(79320-84-6)

Safety Data

• Hazardous Substances Data: 79320-84-6(Hazardous Substances Data)

Usage

General Description

The chemical "(4alpha)-15-(acetyloxy)-3-oxo-12,13-epoxytrichothec-9-en-4-yl chloroacetate" is a synthetic derivative of trichothecene, which is a type of mycotoxin produced by certain fungi. Trichothecenes are known for their potent toxicity and ability to cause a range of adverse health effects. This specific derivative contains an epoxy group and a chloroacetate group, which likely contribute to its toxic and reactive properties. The acetyloxy group may also affect its bioavailability and distribution within the body. Overall, this chemical represents a potentially hazardous substance that should be handled with caution and studied for its potential health impacts.

Upstream product

• 77620-46-3 15-acetoxy-4β-chloroacetoxy-3α-hydroxy-12,13-epoxytrichothec-9-ene 
• 79320-83-5 4β,15-dichloroacetoxy-12,13-epoxytrichothec-9-en-3-one 
• 77620-40-7 4β,15-diacetoxy-3α-O-(2-tetrahydropyranyl)scirpene 
• 77620-42-9 15-acetoxy-3α-O-(2-tetrahydropyranyl)scirpen-4β-ol 
• 77620-60-1 15-acetoxy-4β-(chloroacetoxy)-3α-O-(2-tetrahydropyranyl)scirpene 
• 2270-40-8 anguidine 
• 77620-46-3 15-acetoxy-4β-(chloroacetoxy)scirpen-3α-ol 

Relevant articles and documents

Structural modifications of anguidin and antitumor activities of its analogues

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