About This Item
Produtos recomendados
Nível de qualidade
Ensaio
98%
pf
53-56 °C (lit.)
grupo funcional
iodo
cadeia de caracteres SMILES
Ic1cccnc1
InChI
1S/C5H4IN/c6-5-2-1-3-7-4-5/h1-4H
chave InChI
XDELKSRGBLWMBA-UHFFFAOYSA-N
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Descrição geral
3-Iodopyridine is a heteroaryl halide. It undergoes microwave-assisted coupling with heterocyclic compounds (pyrazole, imidazole, pyrrole and indole) to afford the corresponding N-3-pyridinyl-substituted heterocyclic compounds.
Aplicação
3-Iodopyridine may be used to synthesize following pyridine alkaloids:
- theonelladins C
- theonelladins D
- niphatesine C
- xestamine D
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
224.1 °F - closed cup
Ponto de fulgor (°C)
106.7 °C - closed cup
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of pyridine alkaloids via Pd-catalyzed coupling of 3-iodopyridine, 1, ?-dienes and nitrogen nucleophiles.
Tetrahedron Letters, 43(1), 21-23 (2002)
Organic letters, 6(22), 3897-3899 (2004-10-22)
[reaction: see text] 1,4-Disubstituted 1,2,3-triazoles are obtained in excellent yields by a convenient one-pot procedure from a variety of readily available aromatic and aliphatic halides without isolation of potentially unstable organic azide intermediates.
Physical chemistry chemical physics : PCCP, 19(46), 31072-31084 (2017-11-21)
Small nitrogen containing heteroaromatics are fundamental building blocks for many biological molecules, including the DNA nucleotides. Pyridine, as a prototypical N-heteroaromatic, has been implicated in the chemical evolution of many extraterrestrial environments, including the atmosphere of Titan. This paper reports
Journal of the American Society for Mass Spectrometry, 30(10), 2144-2151 (2019-08-09)
Suzuki cross-coupling is a widely performed reaction, typically using metal catalysts under heated conditions. Acceleration of the Suzuki cross-coupling reaction has been previously explored in microdroplets using desorption electrospray ionization mass spectrometry (DESI-MS). Building upon previous work, presented here is
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