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Merck
CN

553719

Sigma-Aldrich

2-氨基-3-溴吡啶

97%

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About This Item

经验公式(希尔记法):
C5H5BrN2
CAS号:
分子量:
173.01
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

形式

solid

mp

63-67 °C

SMILES字符串

Nc1ncccc1Br

InChI

1S/C5H5BrN2/c6-4-2-1-3-8-5(4)7/h1-3H,(H2,7,8)

InChI key

RBCARPJOEUEZLS-UHFFFAOYSA-N

应用

2-Amino-3-bromopyridine may be used to synthesize:
  • 2-acylamido-3-bromopyridines
  • 2-anilino-3-bromopyridine
  • 3-[(2-methoxyphenyl)ethynyl]pyridin-2-amine
  • 3-[(4-methoxyphenyl)ethynyl]pyridin-2-amine
  • N-(bromopyridyl)amidines
  • carbolines via palladium catalyzed arylation followed by palladium catalyzed amination reaction
  • 2-amino-3-cyanopyridine via palladium catalyzed cyanation reaction with potassium ferro-cyanide in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene [DBU]
  • nitro-substituted N,N′-dipyridinylamines via palladium catalyzed coupling reaction with 2-chloro-3-nitropyridine in the presence of Xantphos ligand
  • 2-amino-3-iodopyridine via reaction with sodium iodide in the presence of copper(I)iodide and trans-N,N′-dimethylcyclohexane-1,2-diamine

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Synthesis of pyridopyrimidines by palladium-catalyzed isocyanide insertion.
Este'vez V, et al.
ACS Catalysis, 4(1), 40-43 (2013)
"Smiles Rearrangement as a Tool for the Preparation of Dihydrodipyridopyrazines"
Patriciu I-O, et al.
Organic Letters, 11(23), 5502-5505 (2009)
Phosphonylation of 2-Amino-and 2-Amido-3-bromopyridines and 2-Amino-3-chloroquinoxalines with Triethyl Phosphite.
Adam M, et al.
European Journal of Organic Chemistry, 27, 4655-4665 (2009)
"Syntheses of pyrido [1, 2-a][1, 3, 5] triazin-4-one C-deoxyribonucleosides"
Oda H, et al.
Tetrahedron, 64(45), 11021-11029 (2007)
Novel synthetic strategy of carbolines via palladium-catalyzed amination and arylation reaction.
Iwaki T, et al.
Journal of the Chemical Society. Perkin Transactions 1, 11, 1505-1510 (1999)

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