113514
2-氨基-3-硝基吡啶
99%
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关于此项目
经验公式（希尔记法）:
C5H5N3O2
化学文摘社编号:
分子量:
139.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-144-0
Beilstein/REAXYS Number:
124468
MDL number:
产品名称
2-氨基-3-硝基吡啶, 99%
InChI key
BPYHGTCRXDWOIQ-UHFFFAOYSA-N
InChI
1S/C5H5N3O2/c6-5-4(8(9)10)2-1-3-7-5/h1-3H,(H2,6,7)
SMILES string
Nc1ncccc1[N+]([O-])=O
assay
99%
form
solid
mp
163-165 °C (lit.)
functional group
nitro
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General description
2-Amino-3-nitropyridine functionalizes Wang resin via a carbamate linkage.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
332.6 °F - closed cup
flash_point_c
167 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Monika Ermann et al.
Journal of combinatorial chemistry, 4(4), 352-358 (2002-07-09)
A solid-phase synthesis of substituted cyclic urea derivatives as potential heterocyclic library scaffolds is described. 2-Amino-3-nitropyridine is attached to Wang resin via a carbamate linkage. Reduction of the nitro group was achieved with SnCl(2).2H(2)O. Reductive alkylation with a range of
Jonita Stankevičiūtė et al.
Scientific reports, 6, 39129-39129 (2016-12-17)
Pyridinols and pyridinamines are important intermediates with many applications in chemical industry. The pyridine derivatives are in great demand as synthons for pharmaceutical products. Moreover, pyridines are used either as biologically active substances or as building blocks for polymers with
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