1384881-77-9

Basic information

• Product Name: C₁₉H₁₉NO₂
• Synonyms: C₁₉H₁₉NO₂
• CAS NO: 1384881-77-9
• Molecular Weight: 293.365
• Mol File: 1384881-77-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: C₁₉H₁₉NO₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₉H₁₉NO₂(1384881-77-9)
• EPA Substance Registry System: C₁₉H₁₉NO₂(1384881-77-9)

Safety Data

• Hazardous Substances Data: 1384881-77-9(Hazardous Substances Data)

Upstream product

• 556-56-9 allyl iodid 
• 6275-26-9 2,2-bis(4-methoxyphenyl)acetonitrile 
• 728-87-0 4,4'-Dimethoxybenzhydrol 
• 623-12-1 4-chloromethoxybenzene 
• 106-95-6 allyl bromide 

Downstream Products

• 1384881-80-4 2,2-bis(4-methoxyphenyl)pent-4-en-1-ol 

Relevant articles and documents

Enantioselective Pd(II)-Catalyzed Intramolecular Oxidative 6- endo Aminoacetoxylation of Unactivated Alkenes

A novel asymmetric 6-endo aminoacetoxylation of unactivated alkenes by palladium catalysis, which yields chiral β-acetoxylated piperidines with excellent chemo-, regio- and enantioselectivities under very mild reaction conditions, has been established herein by employing a new designed pyridine-oxazoline (Pyox) ligand. Importantly, introducing a sterically bulky group into the C-6 position of Pyox is crucial to enhance the reactivity of the aminoacetoxylation of alkenes.

6-azabicyclo[3.2.1]octanes via copper-catalyzed enantioselective alkene carboamination

Bridged bicyclic rings containing nitrogen heterocycles are important motifs in bioactive small organic molecules. An enantioselective copper-catalyzed alkene carboamination reaction that creates bridged heterocycles is reported herein. Two new rings are