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Merck
CN

516392

2-Amino-5-iodopyridine

98%

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About This Item

Empirical Formula (Hill Notation):
C5H5IN2
CAS Number:
Molecular Weight:
220.01
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
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Quality Level

assay

98%

mp

128-131 °C (lit.)

functional group

iodo

SMILES string

Nc1ccc(I)cn1

InChI

1S/C5H5IN2/c6-4-1-2-5(7)8-3-4/h1-3H,(H2,7,8)

InChI key

IVILGUFRMDBUEQ-UHFFFAOYSA-N



pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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N Sundaraganesan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(3-4), 830-836 (2006-10-05)
The Fourier transform Raman and Fourier transform infrared spectra of 2-amino-5-iodopyridine were recorded in the solid phase. The equilibrium geometry, harmonic vibrational frequencies, infrared intensities and Raman scattering activities were calculated by HF and DFT (B3LYP) methods with the 6-31G(d,p)
R J Bochis et al.
Journal of medicinal chemistry, 21(2), 235-237 (1978-02-01)
A series of methyl imidazo-[11,2-a]pyridine-2-carbamates was synthesized for anthelmintic testing. The preparation of this class of compounds was simplified by utilization of a novel one-step condensation of the appropriately substituted 2-aminopyridine and methyl chloroacetylcarbamate. The most potent compound, methyl 6-(phenylsulfinyl)-imidazo[1,2-a]pyridine-2-carbamate
Transition metal halide salts of 2-amino-5-substituted-pyridines: Synthesis, crystal structure and magnetic properties of two polymorphs of (5-IAP)2CuCl4 [5-IAP= 2-amino-5-iodopyridinium].
Giantsidis J, et al.
Journal of Coordination Chemistry, 55(7), 795-803 (2002)



Global Trade Item Number

SKUGTIN
516392-1G04061825754413