A78209
3-氨基吡啶
99%
别名:
3-吡啶胺
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关于此项目
经验公式（希尔记法）:
C5H6N2
化学文摘社编号:
分子量:
94.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-322-2
Beilstein/REAXYS Number:
105692
MDL number:
产品名称
3-氨基吡啶, 99%
InChI key
CUYKNJBYIJFRCU-UHFFFAOYSA-N
InChI
1S/C5H6N2/c6-5-2-1-3-7-4-5/h1-4H,6H2
SMILES string
Nc1cccnc1
assay
99%
form
flakes
bp
248 °C (lit.)
mp
60-63 °C (lit.)
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signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3
target_organs
Respiratory system
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
190.4 °F - closed cup
flash_point_c
88 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
危险化学品
此项目有
Daniel Cappel et al.
Journal of chemical information and modeling, 51(10), 2581-2594 (2011-09-16)
The model binding site of the cytochrome c peroxidase (CCP) W191G mutant is used to investigate the structural and dynamic properties of the water network at the buried cavity using computational methods supported by crystallographic analysis. In particular, the differences
Nitric oxide synthase inhibitor facilitates aminopyridine induced neocortical seizure.
B Boda et al.
Neurobiology (Budapest, Hungary), 4(1-2), 103-104 (1996-01-01)
Jaslin Ikhsan et al.
Journal of colloid and interface science, 284(2), 383-392 (2005-03-23)
The sorption of 2-, 3-, and 4-aminopyridine on K-saturated Wyoming (SWy-K) and Texas (STx-K) and Ca-enriched Texas (STx-Ca) montmorillonite was measured at 25 degrees C with 10 mM KNO(3) or 3.3 mM Ca(NO(3))(2) as the background electrolyte. The aminopyridines adsorbed
Pierre Garcia et al.
Organic letters, 13(8), 2030-2033 (2011-03-19)
Bimolecular cobalt-catalyzed [2 + 2 + 2] cycloadditions between yne-ynamides and nitriles afford bicyclic 3- or 4-aminopyridines in up to 100% yield. The high regioselectivity observed depends on the substitution pattern at the starting ynamide. Aminopyridines bearing TMS and Ts
E O'Hearn et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 17(22), 8828-8841 (1997-11-14)
Ibogaine, an indole alkaloid that causes hallucinations, tremor, and ataxia, produces cerebellar neurotoxicity in rats, manifested by degeneration of Purkinje cells aligned in narrow parasagittal bands that are coextensive with activated glial cells. Harmaline, a closely related alkaloid that excites
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