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2-Amino-3-iodopyridine, 97%|282874|104830-06-0

2-Amino-3-iodopyridine, 97%

Cat. No JK282874_1_G
J&K Chemical

Product Information

Product Name
2-Amino-3-iodopyridine, 97%
Brand Name
J&K
Product Number
282874
CAS
104830-06-0
Molecular Formula
C5H5IN2
Molecular Weight
220.01
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2763151
IUPAC Name
3-iodopyridin-2-amine
InChI Key
UUDNBWSHTUFGDQ-UHFFFAOYSA-N
SMILES
C1=CC(=C(N=C1)N)I

Properties

Melting Point
87-91

Safety Information

GHS Symbols
Hazard Symbol
Hazard Symbol
Signal Word
Danger
Hazard Statement
H302
H315
H318
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P332+P317
P362+P364
P264+P265
P305+P354+P338
P304+P340
P403+P233

References

Recent advances in the synthesis of thiazolo[4,5-b]pyridines. Part 1: Focus on pyridine annulation to thiazole ring (microreview)
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2024-02
DOI: 10.1007/s10593-024-03289-0|10.1007/s10593-024-03307-1

From Halopyridin-2-amines and Alkynes (Larock Synthesis)
Publication Name: Science of Synthesis
Publication Date: 2016

Development of bright fluorescent quadracyclic adenine analogues: TDDFT-calculation supported rational design
Publication Name: Scientific Reports
Publication Date: 2015-07-31
DOI: 10.1038/srep12653

Metal-Catalyzed Cross-Coupling Reactions for Indoles
Publication Name: Topics in Heterocyclic Chemistry
Publication Date: 2010
DOI: 10.1007/7081_2010_36

Efficient Synthesis of 2-Substituted 7-Azaindole Derivatives via Palladium-Catalyzed Coupling and C–N Cyclization Using 18-Crown-6
Publication Name: Synthesis
Publication Date: 2007-06-18
DOI: 10.1055/s-2007-983730

2-Amino-3-iodopyridine, 97%

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