267002-57-3

Basic information

• Product Name: Benzenamine, 4-bromo-2-(2-propenyl)-
• CAS NO: 267002-57-3
• Molecular Formula: C9H10BrN
• Molecular Weight: 212.089
• Mol File: 267002-57-3.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-bromo-2-(2-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-bromo-2-(2-propenyl)-(267002-57-3)
• EPA Substance Registry System: Benzenamine, 4-bromo-2-(2-propenyl)-(267002-57-3)

Safety Data

• Hazardous Substances Data: 267002-57-3(Hazardous Substances Data)

Upstream product

• 22774-76-1 N-allyl-4-bromobenzenamine 
• 131818-17-2 tert-butyl (4-bromophenyl)carbamate 
• 1361121-45-0 C₁₄H₁₈BrNO₂ 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 500872-45-7 (2-allyl-4-bromo-phenylamino)-acetic acid tert-butyl ester 
• 321435-99-8 7-bromo-2,3,4,5-tetrahydro-1H-benzo[b]azepine 
• 1017336-71-8 C₁₀H₁₂BrN 
• 113092-92-5 6-bromo-3-methyl-3,4-dihydroquinolin-2(1H)-one 
• 1361121-50-7 C₉H₁₀BrN 
• 1361121-53-0 C₁₆H₁₆BrNO₂S 
• 1361121-59-6 C₁₉H₁₈BrNO₂S 
• 1374693-98-7 C₂₇H₂₈BrNO₆S 
• 1240273-25-9 2-allyl-N-benzyl-4-bromoaniline 

Relevant articles and documents

One-pot Construction of Difluorinated Pyrrolizidine and Indolizidine Scaffolds via Copper-Catalyzed Radical Cascade Annulation

A convenient approach to the synthesis of diverse difluorinated nitrogen-containing polycycles via a copper-catalyzed radical cascade annulation of amine-containing olefins and ethyl bromodifluoroacetate was developed. Three new bonds, including a Csp3 ?CF2 and two C?N bonds, are forged simultaneously in this strategy. Through this strategy, a series of difluorinated pyrrolizidine and indolizidine derivatives have been conveniently synthesized in good yields. (Figure presented.).

M-CPBA-Mediated Intramolecular Aminohydroxylation of N-Sulfonyl Aminoalkenes to Synthesize β-Hydroxyl Cyclic Amines

A variety of structurally diverse N-sulfonyl-protected aminoalkenes readily reacted with m-CPBA to produce a series of β-hydroxyl cyclic amines in high yields through intramolecular aminohydroxylation. This metal-free and easy-to-handle synthetic methodol

Palladium-catalyzed selective aminoamidation and aminocyanation of alkenes using isonitrile as amide and cyanide sources

A mild and efficient palladium-catalyzed intermolecular aminoamidation and aminocyanation reaction of alkenes with a broad substrate scope has been developed. This cyclization process provides a valuable synthetic tool for obtaining substituted indolines, tetrahydroisoquinolines and pyrrolidines in good to excellent yields. This journal is