33829-88-8

Basic information

• Product Name: 4-bromo-N-(furan-2-ylmethyl)aniline
• Synonyms: 4-bromo-N-(furan-2-ylmethyl)aniline;(4-Bromo-phenyl)-furan-2-ylmethyl-amine
• CAS NO: 33829-88-8
• Molecular Formula: C₁₁H₁₀BrNO
• Molecular Weight: 252.1072
• Mol File: 33829-88-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-bromo-N-(furan-2-ylmethyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-bromo-N-(furan-2-ylmethyl)aniline(33829-88-8)
• EPA Substance Registry System: 4-bromo-N-(furan-2-ylmethyl)aniline(33829-88-8)

Safety Data

• Hazardous Substances Data: 33829-88-8(Hazardous Substances Data)

Upstream product

• 13533-23-8 4-bromo-N-furfurylidene-aniline 
• 98-01-1 furfural 
• 106-40-1 4-bromo-aniline 
• 13533-23-8 C₁₁H₈BrNO 
• 2460-44-8 β-D-xylopyranoside 
• 87-72-9 L-(+)-arabinose 
• 10257-32-6 D-ribose 

Downstream Products

• 95848-40-1 3-(4-Bromo-phenyl)-10-oxa-3-aza-tricyclo[5.2.1.0^1,5]dec-8-ene 
• 114142-98-2 6-[(4-Bromo-phenyl)-furan-2-ylmethyl-amino]-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carbaldehyde 
• 114143-04-3 6-[(4-Bromo-phenyl)-furan-2-ylmethyl-amino]-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carbaldehyde oxime 
• 114143-15-6 11-(4-Bromo-phenyl)-1,3-dimethyl-10,11-dihydro-1H,6aH-6,9-dioxa-1,3,5,11-tetraaza-pentaleno[1,6a-a]naphthalene-2,4-dione 

Relevant articles and documents

One-pot synthesis of amines from biomass resources catalyzed by HReO4

This work describes the one-pot synthesis of furfurylamines from carbohydrates catalyzed by HReO4. These one-pot three-reaction and four-reaction processes allow the conversion of xylose and xylan, respectively, into a large variety of secondary and tertiary amines with good overall yields and chemoselectivity.

Structure-activity relationship study of homoallylamines and related derivatives acting as antifungal agents

The synthesis, in vitro evaluation, and structure-activity relationship studies of homoallylamines and related derivatives acting as antifungal agents are reported. Among them, compounds N-(4-bromophenyl)-N-(2-furylmethyl)amine and N-(4-chlorophenyl)-N-(2