3551-51-7

Basic information

• Product Name: N-(cyclopent-2-en-1-yl)-benzamide
• Synonyms: N-(cyclopent-2-en-1-yl)-benzamide
• CAS NO: 3551-51-7
• Molecular Weight: 187.241
• Mol File: 3551-51-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(cyclopent-2-en-1-yl)-benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(cyclopent-2-en-1-yl)-benzamide(3551-51-7)
• EPA Substance Registry System: N-(cyclopent-2-en-1-yl)-benzamide(3551-51-7)

Safety Data

• Hazardous Substances Data: 3551-51-7(Hazardous Substances Data)

Upstream product

• 3350-06-9 2-cyclopentenamine 
• 98-88-4 benzoyl chloride 
• 285-67-6 Cyclopentene oxide 
• 285-63-2 6-azabicyclo<3.1.0>hexane 
• 18762-60-2 6-benzoyl-6-azabicyclo<3.1.0>hexane 
• 698-16-8 benzohydroximoyl chloride 
• 142-29-0 cyclopentene 
• 78607-65-5 N-benzoyl-2-aza-3-oxabicyclo(2.2.1)heptane 

Downstream Products

• 50401-81-5 N-Allyl-N-cyclopent-2-enyl-benzamide 
• 127310-82-1 6-benzamido-3-phenyl-3aα,5,6α,6aα-tetrahydro-4H-cyclopentisoxazole 
• 127310-97-8 4-benzamido-3-phenyl-3aα,5,6,6aα-tetrahydro-4βH-cyclopentisoxazole 
• 6094-36-6 N-benzoylglutamic acid 
• 617-65-2 Glutamic acid 
• 127311-22-2 6-(N-methyl)benzamido-3-tert-butyl-3aα,5,6α,6aα-tetrahydro-4H-cyclopentisoxazole 
• 127311-22-2 6-(N-methyl)benzamido-3-tert-butyl-3aα,5,6β,6aα-tetrahydro-4H-cyclopentisoxazole 
• 127311-23-3 4-(N-methyl)benzamido-3-tert-butyl-3aα,5,6,6aα-tetrahydro-4βH-cyclopentisoxazole 
• 127310-74-1 N-(cyclopent-2-en-1-yl)-N-methylbenzamide 
• 127311-07-3 6-benzamido-3-tert-butyl-3aα,5,6α,6aα-tetrahydro-4H-cyclopentisoxazole 
• 127311-17-5 4-benzamido-3-tert-butyl-3aα,5,6,6aα-tetrahydro-4βH-cyclopentisoxazole 
• 127311-07-3 6-benzamido-3-tert-butyl-3aα,5,6β,6aα-tetrahydro-4H-cyclopentisoxazole 

Relevant articles and documents

The Easy Approach to N -Hydroxy- N -cycloalkenylamides through Nitrosocarbonyl Ene Reactions to Cycloalkenes: Valuable Compounds for Antiviral Syntheses

An easy approach to N -hydroxy- N -cycloalkenylamides, ene adducts of cyclic alkenes of different sizes, is presented. The products can be obtained both through the thermal generation of the nitrosocarbonyl intermediates and via the photochemical fragment

HYDROGEN BOND DIRECTED NITRILE OXIDE CYCLOADDITION REACTIONS OF ALLYLIC 2o-AMIDES

The ability of allylic and homoallylic 2o-amides to direct nitrile oxide cycloaddition reactions has been studied.For N-cyclopentenyl amides, good regio- and stereochemical control are observed and mechanistic studies suggest that hydrogen bond