119952-14-6

Basic information

• Product Name: C₂₄H₂₅NO
• Synonyms: C₂₄H₂₅NO
• CAS NO: 119952-14-6
• Molecular Weight: 343.469
• Mol File: 119952-14-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₂₄H₂₅NO(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₄H₂₅NO(119952-14-6)
• EPA Substance Registry System: C₂₄H₂₅NO(119952-14-6)

Safety Data

• Hazardous Substances Data: 119952-14-6(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 144863-35-4 Verbenone benzylamine imine 
• 18309-32-5 Verbenone 
• 609-67-6 2-Iodobenzoyl chloride 
• 119952-13-5 N-Benzyl-N-((1R,5S)-6,6-dimethyl-4-methylene-bicyclo[3.1.1]hept-2-en-2-yl)-2-iodo-benzamide 
• 121359-48-6 2-(tri-n-butylstannyl)thiazole 
• 119952-13-5 N-Benzyl-N-(6,6-dimethyl-4-methylene-bicyclo[3.1.1]hept-2-en-2-yl)-2-iodo-benzamide 
• 119952-13-5 N-Benzyl-N-((1S,5R)-6,6-dimethyl-4-methylene-bicyclo[3.1.1]hept-2-en-2-yl)-2-iodo-benzamide 

Relevant articles and documents

Palladium Catalysed Tandem Cyclisation-Anion Capture Processes. Part 1. Background and Hydride Ion Capture by Alkyl- and ?-Allyl-Palladium Species.

A new, wide ranging, synthetically powerful, catalytic tandem cyclisation-anion capture process is proposed which depends on the rate of cyclisation of an organopalladium specifies (RPdX) onto a proximate alkene or diene being significantly faster than an

PALLADIUM CATALYSED TANDEM CYCLISATION-ANION CAPTURE PROCESSES. HYDRIDE ION CAPTURE BY ALKYL- AND ?-ALLYL-PALLADIUM SPECIES

Alkyl- and ?-allyl-palladium species arising from 5-exo-trig cyclisation onto proximate alkenes or dienes can be intercepted by hydride ion sources leading to carbo- and hetero-cyclic compounds usually in good yield.