4780-17-0

Basic information

• Product Name: 3-[(2,4-dichlorophenoxy)methyl]-5-phenyl-1,2,4-oxadiazole
• CAS NO: 4780-17-0
• Molecular Formula: C₁₅H₁₉NO₁₀
• Molecular Weight: 321.1581
• Mol File: 4780-17-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 479.1°C at 760 mmHg
• Flash Point: 243.6°C
• Density: 1.38g/cm³
• Vapor Pressure: 7.05E-09mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: 3-[(2,4-dichlorophenoxy)methyl]-5-phenyl-1,2,4-oxadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(2,4-dichlorophenoxy)methyl]-5-phenyl-1,2,4-oxadiazole(4780-17-0)
• EPA Substance Registry System: 3-[(2,4-dichlorophenoxy)methyl]-5-phenyl-1,2,4-oxadiazole(4780-17-0)

Safety Data

• Hazardous Substances Data: 4780-17-0(Hazardous Substances Data)

Upstream product

• 75-44-5 phosgene 
• 5432-46-2 1,3,4,6-tetra-O-acetyl-D-glucosamine hydrochloride 
• 14131-63-6 D-glucosamine hydrochloride 
• 51471-40-0 6-(hydroxymethyl)-3-[4-methoxybenzylideneamino]tetrahydropyran-2,4,5-triol 
• 32315-10-9 bis(trichloromethyl) carbonate 

Downstream Products

• 149117-44-2 2-deoxy-2-<3-(4-tolylureido)>-α-D-glucopyranose 
• 149117-41-9 C₁₃H₁₇ClN₂O₆ 
• 149117-40-8 2-<3-(4-chlorophenylureido)>-2-deoxy-α-D-glucopyranose 
• 149117-59-9 (4R,5R)-4-(D-arabino-tetritol-1-yl)-1-(4-chlorophenyl)-5-hydroxyimidazolidin-2-one 

Relevant articles and documents

Acetyl glucosamine imidazolemethanol -2, 4, 5-Trion synthetic method of use with bacteriostatic

The invention discloses acetylglucosamine imidazol-2,4,5-trione, and further discloses a synthetic method of the acetylglucosamine imidazol-2,4,5-trione and antimicrobial application. The synthetic method is quick, efficient and high in productivity, and

Synthesis of novel glycosyl imidazolidine-2,4,5-trione derivatives

A series of glycosyl imidazolidine-2,4,5-trione derivatives were achieved by condensing per-O-acetylated glucosamine, triphosgene, amines and oxalyl chloride. The convenient and efficient method afforded the desired products with good to excellent yields

Synthesis of sugar isocyanates and their application to the formation of ureido-linked disaccharides

The present work describes a facile and practical route to carbohydrate-based isocyanates, a reactive and appealing family of chiral heterocumulenes, wich can be easily converted into disaccharides and pseudodisaccharides interconnected by urea moieties.