6931-11-9

Basic information

• Product Name: 3,4-Dihydro-3,3,5-trimethyl-2H-pyrrole 1-oxide
• Synonyms: 2,4,4-Trimethyl-1-pyrroline 1-oxide;3,4-Dihydro-3,3,5-trimethyl-2H-pyrrole 1-oxide
• CAS NO: 6931-11-9
• Molecular Formula: C₇H₁₃NO
• Molecular Weight: 127.1842
• Mol File: 6931-11-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 196.6°Cat760mmHg
• Flash Point: 71.6°C
• Appearance: /
• Density: 0.94g/cm³
• Vapor Pressure: 0.555mmHg at 25°C
• Refractive Index: 1.474
• CAS DataBase Reference: 3,4-Dihydro-3,3,5-trimethyl-2H-pyrrole 1-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Dihydro-3,3,5-trimethyl-2H-pyrrole 1-oxide(6931-11-9)
• EPA Substance Registry System: 3,4-Dihydro-3,3,5-trimethyl-2H-pyrrole 1-oxide(6931-11-9)

Safety Data

• Hazardous Substances Data: 6931-11-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H13NO/c1-6-4-7(2,3)5-8(6)9/h4-5H2,1-3H3

Upstream product

• 913260-88-5 2,2-dimethylpenta-3,4-dienal oxime 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 35223-73-5 4,4-dimethyl-5-nitropentan-2-one 

Downstream Products

• 108622-94-2 3,3-dimethyl-5-(4-nitro-trans-styryl)-3,4-dihydro-2H-pyrrole-1-oxide 
• 72700-89-1 3,3-dimethyl-5-trans-styryl-3,4-dihydro-2H-pyrrole-1-oxide 
• 111719-58-5 5-Benzamido-1-benzoyloxy-4,4-dimethyl-pentan-2-on 
• 30406-95-2 5-benzoylamino-3-benzoyloxy-4,4-dimethyl-pentan-2-one 
• 50455-67-9 6,6,7a-trimethyl-1-phenyl-tetrahydro-pyrrolo[1,2-b][1,2,4]oxadiazole-2-thione 
• 597-43-3 2,2-dimethylsuccinic acid 
• 119099-18-2 (1-Ethoxy-2,4,4-trimethyl-pyrrolidin-2-yl)-phenyl-phosphinic acid ethyl ester 
• 93-98-1 N-phenyl benzoyl amide 
• 95755-14-9 2-(N-benzoyl-N-phenylaminomethyl)-4,4-dimethyl-Δ¹-pyrroline 
• 1072938-37-4 6,6,7a-trimethyl-1-phenyltetrahydropyrrolo[1,2-b][1,2,4]oxadiazol-2(1H)-one 
• 64760-49-2 1-hydroxy-2-isobutenyl-2,4,4-trimethyl-5-phenylpyrrolidine 
• 64760-49-2 1-hydroxy-2-isobutenyl-2,4,4-trimethyl-5-phenylpyrrolidine 
• 355019-36-2 3-[buta-1(E),3-dienyl]-2-phenyl-3a,5,5-trimethyl-3a,4,5,6-tetrahydropyrrolo[1,2-b]isoxazole 
• 560131-73-9 C₁₆H₁₉NO₂ 

Relevant articles and documents

Allenyloxime-a new source of heterocyclizations to stable cyclic nitrones

A variety of conditions including reductive and/or basic reagents in aqueous or alcoholic solution was applied to 2,2-dimethylpenta-3,4-dienal oxime. Formation of various five-membered heterocycles with excellent chemical selectivity was observed. Most of the reactions yielded cyclic nitrones with stable dipolar structure and unique functionalities present. All products of cyclization were isolated and fully characterized.