59171-91-4

Basic information

• Product Name: 3,5-Cycloheptadien-1-ol, benzoate
• CAS NO: 59171-91-4
• Molecular Formula: C14H14O2
• Molecular Weight: 214.264
• Mol File: 59171-91-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,5-Cycloheptadien-1-ol, benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Cycloheptadien-1-ol, benzoate(59171-91-4)
• EPA Substance Registry System: 3,5-Cycloheptadien-1-ol, benzoate(59171-91-4)

Safety Data

• Hazardous Substances Data: 59171-91-4(Hazardous Substances Data)

Upstream product

• 94427-72-2 1,8-nonadiene-5-ol 
• 1466415-62-2 nona-1,8-dien-5-yl benzoate 

Downstream Products

• 95687-94-8 Benzoic acid (1R,3R,6S)-3-amino-6-hydroxy-cycloheptyl ester; hydrochloride 
• 95687-96-0 Benzoic acid (1R,3R,6R)-3-chloro-6-ethoxycarbonylamino-cycloheptyl ester 
• 95687-95-9 Benzoic acid (1R,3R,6S)-3-ethoxycarbonylamino-6-hydroxy-cycloheptyl ester 
• 18470-33-2 Nortropacocaine 
• 537-26-8 tropacocain 
• 135-97-7 pseudotropine 
• 95687-99-3 bis(all-cis-3-(benzoyloxy)-5-(<(benzyloxy)-carbonyl>amino)cycloheptyl) sulfite 
• 95799-02-3 bis(all-cis-3-(benzoyloxy)-5-<(ethoxycarbonyl)amino>cycloheptyl)sulfite 
• 95687-94-8 all-cis-5-amino-3-(benzoyloxy)cycloheptanol hydrochloride 
• 95687-97-1 3β-(benzoyloxy)-1β(<(benzyloxy)carbonyl>amino)-5α-chlorocycloheptane 
• 95687-98-2 all-cis-3-(benzoyloxy)-5-(<(benzyloxy)carbonyl>amino)-cycloheptanol 
• 95687-96-0 3β-(benzoyloxy)-5α-chloro-1β-<(ethoxycarbonyl)amino>cycloheptane 
• 95687-95-9 all-cis-3-(benzoyloxy)-5-<(ethoxycarbonyl)amino>cycloheptanol 
• 95687-87-9 N-<(benzyloxy)carbonyl>nortropacocaine 

Relevant articles and documents

Synthesis of 1,3-Cycloalkadienes from Cycloalkenes: Unprecedented Reactivity of Oxoammonium Salts

Few methods allow for the direct conversion of cycloalkenes into cycloalkadienes with high chemo- and regioselectivity. Herein, we report a convenient one-pot process for this transformation that involves the unprecedented N-preferential group transfer of N-oxoammonium salts to cycloalkenes, followed by Cope elimination, to afford cycloalkadienes at room temperature and pressure.