95687-91-5

Basic information

• Product Name: Benzamide, N-(4-hydroxycycloheptyl)-, cis-
• CAS NO: 95687-91-5
• Molecular Formula: C14H19NO2
• Molecular Weight: 233.31
• Mol File: 95687-91-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzamide, N-(4-hydroxycycloheptyl)-, cis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(4-hydroxycycloheptyl)-, cis-(95687-91-5)
• EPA Substance Registry System: Benzamide, N-(4-hydroxycycloheptyl)-, cis-(95687-91-5)

Safety Data

• Hazardous Substances Data: 95687-91-5(Hazardous Substances Data)

Upstream product

• 115522-50-4 N-<4-Hydroxy-cycloheptyl>-p-toluolsulfonamid 
• 98-88-4 benzoyl chloride 
• 5452-35-7 cycloheptanamine 
• 80-30-8 N-cyclohexyl-p-toluenesulfonamide 
• 16801-70-0 N-cycloheptyl-4-methylbenzenesulfonamide 
• 16801-64-2 4-methyl-N-(4-oxo-cyclohexyl)benzenesulfonamide 
• 16801-71-1 N-(4-Oxo-cycloheptyl)-p-toluolsulfonamid 
• 95687-90-4 N-((1S,4R)-4-Hydroxy-cyclohept-2-enyl)-benzamide 
• 95205-45-1 5-{(3aR,5S,6S,6aR)-5-(tert-Butyl-dimethyl-silanyloxy)-6-[(E)-(R)-3-(tert-butyl-dimethyl-silanyloxy)-oct-1-enyl]-1,3a,4,5,6,6a-hexahydro-pentalen-2-yl}-pentanoic acid 
• 95687-90-4 cis-4-(benzoylamino)-2-cycloheptenol 
• 95687-88-0 N-benzoyl-8-oxa-9-azabicyclo<3.2.2>non-6-ene 
• 876938-53-3 Cyclohepta-1,3-diene 
• 495-18-1 Benzohydroxamic acid 

Downstream Products

• 95687-92-6 cis-4-(benzoylamino)-1-<(methylsulfonyl)oxy>cycloheptane 
• 280-05-7 8-azabicyclo[3.2.1]octane 
• 19079-79-9 8-benzyl-8-azabicyclo[3.2.1]octane 
• 113340-10-6 trans-1-(benzylamino)-4-chlorocycloheptane HCl 
• 95687-85-7 (8-azabicyclo[3.2.1]octan-8-yl)(phenyl)methanone 
• 95687-85-7 8-benzoyl-8-azabicyclo<3.2.1>octane 
• 14156-24-2 N-(4-Oxo-cycloheptyl)-benzamide 
• 95687-93-7 trans-1-(benzoylamino)-4-chlorocycloheptane 
• 113340-09-3 cis-4-(benzylamino)cycloheptanol 
• 95687-92-6 Methanesulfonic acid (1R,4S)-4-benzoylamino-cycloheptyl ester 
• 95687-93-7 N-((1S,4S)-4-Chloro-cycloheptyl)-benzamide 

Relevant articles and documents

Synthetic Approaches to Nortropanes and Nortrop-6-enes; Intramolecular Displacement by Nitrogen in 7-Membered Rings

The synthesis of simple nortropane and nortrop-6-ene derivatives from cyclohepta-1,3-diene is described.The key intermediates are trans-1-amino-4-chloro-cycloheptanes and -cyclohept-2-enes which are derived efficiently from the corresponding cis-amino-alcohols and undergo intramolecular cyclisation.Corresponding derivatisation of cyclohexa- and cycloocta-1,3-dienes is explored and attempts to achieve Pd-catalysed cyclisation of 1-amino-4-acetoxy-derivatives is described.Nitrogen inversion data for selected nortropane derivatives are included. Key Words: nortropanes/enes; 1,4-disubstitute cyclohexanes, cycloheptanes, cyclooctanes and -enes; intramolecular cyclisation; slow nitrogen inversion.

A new synthetic route to tropane alkaloids based on [4 + 2] nitroso cycloaddition to 1,3-cycloheptadienes

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