1416969-41-9

Basic information

• Product Name: N-mesitoyl-3,3-dimethyl-5-acetoxy-1,2-isoxazolidine
• Synonyms: N-mesitoyl-3,3-dimethyl-5-acetoxy-1,2-isoxazolidine
• CAS NO: 1416969-41-9
• Molecular Weight: 305.374
• Mol File: 1416969-41-9.mol

Chemical Properties

• CAS DataBase Reference: N-mesitoyl-3,3-dimethyl-5-acetoxy-1,2-isoxazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: N-mesitoyl-3,3-dimethyl-5-acetoxy-1,2-isoxazolidine(1416969-41-9)
• EPA Substance Registry System: N-mesitoyl-3,3-dimethyl-5-acetoxy-1,2-isoxazolidine(1416969-41-9)

Safety Data

• Hazardous Substances Data: 1416969-41-9(Hazardous Substances Data)

Upstream product

• 1416969-33-9 N-mesitoyl-3,3-dimethyl-5-hydroxy-1,2-isoxazolidine 
• 75-36-5 acetyl chloride 
• 40188-34-9 2,4,6-trimethylbenzaldehyde oxime 
• 2904-57-6 mesitylenecarbonitrile oxide 
• 108-24-7 acetic anhydride 
• 556-82-1 3-methyl-2-buten-1-ol 

Downstream Products

• 1416969-43-1 C₁₉H₂₃N₃O₄ 
• 1416969-44-2 C₁₉H₂₂FN₃O₄ 
• 1416969-45-3 C₁₉H₂₂ClN₃O₄ 
• 1416969-46-4 C₁₉H₂₂BrN₃O₄ 
• 1416969-47-5 C₁₉H₂₂IN₃O₄ 
• 1416969-48-6 C₂₀H₂₅N₃O₄ 
• 1416969-49-7 C₁₉H₂₄N₄O₃ 
• 1448227-77-7 6-chloro-9-[2-(mesitylcarbonyl)-3,3-dimethylisoxazolidin-5-yl]-9H-purine 
• 1448227-78-8 6-chloro-7-[2-(mesitylcarbonyl)-3,3-dimethylisoxazolidin-5-yl]-7H-purine 
• 1448227-79-9 2-amino-9-[2-(mesitylcarbonyl)-3,3-dimethylisoxazolidin-5-yl]-1,9-dihydro-6H-purin-6-one 

Relevant articles and documents

From the ene reaction of nitrosocarbonyl intermediates with 3-methylbut-2-En-1-Ol, a new class of purine N,O-nucleoside analogues

Sterically encumbered nitrosocarbonyl derivatives of mesitylene or anthracene undergo ene reactions with 3-methylbut-2-en-1-ol to give the corresponding the 5-hydroxyisoxazolidine adducts in fair yields. According to the proposed mechanism, these heterocy

N, O -nucleosides from ene reactions of nitrosocarbonyl intermediates with the 3-methyl-2-buten-1-ol

Nitrosocarbonyl intermediates undergo ene reactions with allylic alcohols, affording regioisomeric adducts in fair yields. Nitrosocarbonyl benzene reacts with 3-methyl-2-buten-1-ol and follows a Markovnikov orientation and abstracts preferentially the twi