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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:
4214-75-9
分子量:
139.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24846882
EC Number:
224-144-0
Beilstein/REAXYS Number:
124468
MDL number:
MFCD00006314
Assay:
99%
Form:
solid
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assay

99%

form

solid

mp

163-165 °C (lit.)

functional group

nitro

SMILES string

Nc1ncccc1[N+]([O-])=O

InChI

1S/C5H5N3O2/c6-5-4(8(9)10)2-1-3-7-5/h1-3H,(H2,6,7)

InChI key

BPYHGTCRXDWOIQ-UHFFFAOYSA-N

General description

2-Amino-3-nitropyridine functionalizes Wang resin via a carbamate linkage.

pictograms

Exclamation mark
GHS07

signalword

Warning

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
STBJ7162
STBF8949V
STBF7238V
STBF6336V
MKBL7958V

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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

全球贸易项目编号

货号GTIN
113514-25G04061838345226
113514-5G04061832544557