1198297-99-2

Basic information

• Product Name: C₁₀H₉BrN₂O
• Synonyms: C₁₀H₉BrN₂O
• CAS NO: 1198297-99-2
• Molecular Weight: 253.098
• Mol File: 1198297-99-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: C₁₀H₉BrN₂O(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₀H₉BrN₂O(1198297-99-2)
• EPA Substance Registry System: C₁₀H₉BrN₂O(1198297-99-2)

Safety Data

• Hazardous Substances Data: 1198297-99-2(Hazardous Substances Data)

Upstream product

• 1752-88-1 tetrahydro-3H-pyrazol-3-one hydrochloride 
• 6630-33-7 ortho-bromobenzaldehyde 
• 10234-72-7 pyrazolidin-3-one 
• 292638-85-8 acrylic acid methyl ester 

Relevant articles and documents

Photocatalytic reductive radical-radical coupling of: N, N ′-cyclicazomethine imines with difluorobromo derivatives

A visible-light-induced difluoroalkylation of N,N′-cyclicazomethine imine was successfully realized through a novel photoredox radical-radical cross-coupling reaction. This developed protocol exhibits high functional group tolerance and affords a variety

Phosphine-catalyzed [3+2] cycloaddition reactions of azomethine imines with electron-deficient alkenes: A facile access to dinitrogen-fused heterocycles

An efficient method for the phosphine-catalyzed [3+2] cycloaddition reaction of azomethine imines with diphenylsulfonyl alkenes to give dinitrogen-fused bi- or tricyclic heterocyclic compounds in high yields has been described. Moreover, two phenylsulfony

Copper(I) acetate-catalyzed cycloaddition between azomethine imines and propiolates under additive-free conditions

Because propiolates easily undergo base-catalyzed self-Michael addition, most popular catalytic systems in CuAAC cannot be used in the cycloaddition between azomethine imines and propiolates, because such reactions usually require the use of tertiary amin