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4-Amino-3-nitropyridine, 98%|255351|1681-37-4

4-Amino-3-nitropyridine, 98%

Cat. No JK255351_1_G
J&K Chemical

Product Information

Product Name
4-Amino-3-nitropyridine, 98%
Brand Name
J&K
Product Number
255351
CAS
1681-37-4
Molecular Formula
C5H5N3O2
Molecular Weight
139.11
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
3-Nitro-4-pyridinamine
PubChem CID
548803
IUPAC Name
3-nitropyridin-4-amine
InChI Key
IUPPEELMBOPLDJ-UHFFFAOYSA-N
SMILES
C1=CN=CC(=C1N)N+(=O)O-

Properties

Melting Point
203-207

Safety Information

Signal Word
Warning
Hazard Statement
H302
H315
H319
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

Amifampridine
Publication Name: Pharmaceutical Substances
Publication Date: 2020

Synthesis of 4-nitro-γ-carbolines by Graebe–Ullmann reaction
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2019-09
DOI: 10.1007/s10593-019-02547-w

A short and safe method for the synthesis of [1,2,5]oxadiazolo[3,4-c] pyridine
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2015-02
DOI: 10.1007/s10593-015-1683-8

Use of the Graebe-Ullmann reaction in the synthesis of 8-methyl-γ-carboline and isomeric aromatic aza-γ-carbolines
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2012-11-08
DOI: 10.1007/s10593-012-1127-7

Preparation of Novel 2,3,8-Trisubstituted Pyrido[3,4-b]pyrazines and Pyrido[2,3-b]pyrazines
Publication Name: Synthesis
Publication Date: 2011-01-31
DOI: 10.1055/s-0030-1259429

4-Amino-3-nitropyridine, 98%

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