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Merck
모든 사진(2)

주요 문서

441503

Sigma-Aldrich

1-Aminopyridinium iodide

97%

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About This Item

실험식(Hill 표기법):
C5H7IN2
CAS Number:
Molecular Weight:
222.03
Beilstein:
3713241
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

97%

mp

159-161 °C (lit.)

저장 온도

2-8°C

SMILES string

[I-].N[n+]1ccccc1

InChI

1S/C5H7N2.HI/c6-7-4-2-1-3-5-7;/h1-5H,6H2;1H/q+1;/p-1

InChI key

NDRLPYIMWROJBG-UHFFFAOYSA-M

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일반 설명

1-Aminopyridinium iodide, a pyridine derivative, is an important reagent for organic synthesis. It has various pharmaceutical applications. It participates in homogeneous transition metal-catalyzed reactions. Single-crystal X-ray diffraction studies suggest that the compound crystallizes in the monoclinic space group P21/c (phase II). Aza-ylide derived from 1-aminopyridinium iodide serves as a commercially available ammonia equivalent during the preparation of primary amines.

애플리케이션

1-Aminopyridinium iodide may be used in the preparation of room temperature ionic liquids (organic salts in liquid state at room temperature). It may also be used for the preparation of oligomycin A annelated with pyrazolo[1,5-a]pyridine.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

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문서 라이브러리 방문

Lyudmila N Lysenkova et al.
The Journal of antibiotics, 63(1), 17-22 (2009-11-17)
The first examples of chemical modification of antibiotic oligomycin A are described. The interaction of oligomycin A with hydroxylamine yielded six-membered nitrone annelated with the antibiotic at the positions 3,4,5,6,7. The reaction with 1-aminopyridinium iodide in pyridine led to pyrazolo[1,5-a]pyridine
P Andrew Evans et al.
Journal of the American Chemical Society, 131(25), 8722-8723 (2009-06-09)
The transition metal catalyzed allylic amination represents a powerful and versatile cross-coupling for the asymmetric construction of stereogenic C-N bonds that are present in secondary metabolites and medicinally important agents. We have developed a regio- and enantiospecific rhodium-catalyzed allylic amination
Crystal structure and characterization of a novel ferroelastic ionic crystal: 1-Aminopyridinium iodide (C 5 H 7 N 2)+ I-.
Owczarek M, et al.
Chemical Physics Letters, 537, 38-47 (2012)
Supported room temperature ionic liquid membranes for CO2/CH4 separation.
Iarikov DD, et al.
Chemical Engineering Journal, 166(1), 401-406 (2011)

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