推荐产品
等级
analytical standard
质量水平
产品线
PESTANAL®
方案
98-100% (GC)
保质期
limited shelf life, expiry date on the label
技术
HPLC: suitable
gas chromatography (GC): suitable
沸点
204-210 °C (lit.)
mp
54-58 °C (lit.)
应用
agriculture
environmental
包装形式
neat
SMILES字符串
Nc1ccccn1
InChI
1S/C5H6N2/c6-5-3-1-2-4-7-5/h1-4H,(H2,6,7)
InChI key
ICSNLGPSRYBMBD-UHFFFAOYSA-N
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相关类别
一般描述
2-Aminopyridine can be called as structural motifs, which can be encountered in a variety of useful compounds, that includes fluorescent organic materials and therapeutics. It can undergo condensation with an aromatic aldehyde to give the corresponding schiff′s base.
应用
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
推荐产品
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
法律信息
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语:
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
197.6 °F - closed cup
闪点(°C)
92 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
危险化学品
A novel approach towards design, synthesis and evaluation of some Schiff base analogues of 2-aminopyridine and 2-aminobezothiazole against hepatocellular carcinoma
Biomedicine and Pharmacotherapy, 89, 162-176 (2017)
Pd?PEPPSI?IPentCl: A Useful Catalyst for the Coupling of 2?Aminopyridine Derivatives
Chemistry?A European Journal , 23, 3206-3212 (2017)
The Journal of chemical physics, 133(6), 064302-064302 (2010-08-17)
2-Aminopyridine dimer has frequently been used as a model system for studying photochemistry of DNA base pairs. We examine here the relevance of 2-aminopyridine dimer for a Watson-Crick adenine-thymine base pair by studying UV-light induced photodynamics along two main hydrogen
Journal of medicinal chemistry, 52(14), 4533-4537 (2009-06-23)
A common dichotomy exists in inhibitor design: should the compounds be designed to block the enzymes of animals in the preclinical studies or to inhibit the human enzyme? We report that a single mutation of Leu-337 in rat neuronal nitric
The Journal of chemical physics, 136(17), 174308-174308 (2012-05-16)
The S(1)/S(2) state exciton splittings of symmetric doubly hydrogen-bonded gas-phase dimers provide spectroscopic benchmarks for the excited-state electronic couplings between UV chromophores. These have important implications for electronic energy transfer in multichromophoric systems ranging from photosynthetic light-harvesting antennae to photosynthetic
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