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36685

Supelco

2-Aminopyridine

PESTANAL®, analytical standard

Sinonimo/i:

2-AP, 2-Pyridinamine, 2-Pyridylamine

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About This Item

Formula empirica (notazione di Hill):
C5H6N2
Numero CAS:
504-29-0
Peso molecolare:
94.11
Beilstein:
105785
Numero CE:
207-988-4
Numero MDL:
MFCD00006312
Codice UNSPSC:
41116107
ID PubChem:
329755451
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Saggio

98-100% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

P. eboll.

204-210 °C (lit.)

Punto di fusione

54-58 °C (lit.)

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

Nc1ccccn1

InChI

1S/C5H6N2/c6-5-3-1-2-4-7-5/h1-4H,(H2,6,7)
ICSNLGPSRYBMBD-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Prodotti consigliati

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.

Note legali

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Skull and crossbonesCorrosion
GHS06,GHS05

Avvertenze

Danger

Indicazioni di pericolo

H301 + H311,H314,H412

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

197.6 °F - closed cup

Punto d’infiammabilità (°C)

92 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
BCCH4977
BCCC8118
BCBW1271
BCBT7385
SZBC130XV

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Pd?PEPPSI?IPentCl: A Useful Catalyst for the Coupling of 2?Aminopyridine Derivatives
Khadra A, et al.
Chemistry?A European Journal, 23, 3206-3212 (2017)
A novel approach towards design, synthesis and evaluation of some Schiff base analogues of 2-aminopyridine and 2-aminobezothiazole against hepatocellular carcinoma
Chacko S and Samanta S
Biomedicine and Pharmacotherapy, 89, 162-176 (2017)
Honggen Wang et al.
Journal of the American Chemical Society, 132(38), 13217-13219 (2010-09-09)
A novel and efficient synthesis of pyrido[1,2-a]benzimidazoles through direct intramolecular aromatic C-H amination of N-aryl-2-aminopyridines has been developed. The reaction, cocatalyzed by Cu(OAc)(2) and Fe(NO(3))(3)·9H(2)O, is carried out in DMF under a dioxygen atmosphere. Diversified pyrido[1,2-a]benzimidazoles containing various substitution patterns
Thomas Zengeya et al.
Angewandte Chemie (International ed. in English), 51(50), 12593-12596 (2012-11-06)
Peptide nucleic acids containing thymidine and 2-aminopyridine (M) nucleobases form stable and sequence-selective triple helices with double-stranded RNA at physiologically relevant conditions. The M-modified PNA showed unique RNA selectivity by having two orders of magnitude higher affinity for the double-stranded
Philipp Ottiger et al.
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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