2-Amino-3-nitropyridine, 99%

Name: 2-Amino-3-nitropyridine, 99% | 4214-75-9
Brand: J&K Chemical
SKU: JK289006_100_G
Price: 498.8 USD
Availability: InStock

Cat. No JK289006_100_G

Vendor: J&K Chemical

Product Information

Product Name

2-Amino-3-nitropyridine, 99%

Brand Name

J&K

Product Number

289006

CAS

4214-75-9

Molecular Formula

C5H5N3O2

Molecular Weight

139.11

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

77887

IUPAC Name

3-nitropyridin-2-amine

InChI Key

BPYHGTCRXDWOIQ-UHFFFAOYSA-N

SMILES

C1=CC(=C(N=C1)N)N+(=O)O-

Properties

Melting Point

163-165

Flash Point

167

Safety Information

Signal Word

Warning

Hazard Statement

H315

H319

H335

Precautionary Statement

P280

P321

P261

P271

P319

P405

P501

P302+P352

P332+P317

P362+P364

P264+P265

P305+P351+P338

P337+P317

P304+P340

P403+P233

References

Reactivity of 2-aminopyridine N-oxides

Publication Name: Russian Chemical Bulletin

Publication Date: 2024-01

DOI: 10.1007/s11172-024-4120-2

Synthesis and reactivity of furoxano[3,4-b]pyridines (microreview)

Publication Name: Chemistry of Heterocyclic Compounds

Publication Date: 2023-05

DOI: 10.1007/s10593-023-03187-x

Synthesis and nucleophilic dearomatization of highly electrophilic [1,2,5]selenadiazolo[3,4-b]pyridines

Publication Name: Russian Chemical Bulletin

Publication Date: 2022-08

DOI: 10.1007/s11172-022-3596-x

Fragment-based discovery of a new class of inhibitors targeting mycobacterial tRNA modification

Publication Name: Nucleic Acids Research

Publication Date: 2020-06-30

DOI: 10.1093/nar/gkaa539

Investigation of the effects of the proton transfer salts of 2-aminopyridine derivatives with 5-sulfosalicylic acid and their Cu(II) complexes on cancer-related carbonic anhydrases: CA IX and CA XII

Publication Name: Chemical Papers

Publication Date: 2020-02-07

DOI: 10.1007/s11696-020-01078-5

2-Amino-3-nitropyridine, 99%

Product Information

General Information

Properties

Safety Information

References

Reactivity of 2-aminopyridine N-oxides

Synthesis and reactivity of furoxano[3,4-b]pyridines (microreview)

Synthesis and nucleophilic dearomatization of highly electrophilic [1,2,5]selenadiazolo[3,4-b]pyridines

Fragment-based discovery of a new class of inhibitors targeting mycobacterial tRNA modification

Investigation of the effects of the proton transfer salts of 2-aminopyridine derivatives with 5-sulfosalicylic acid and their Cu(II) complexes on cancer-related carbonic anhydrases: CA IX and CA XII