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V900654

Sigma-Aldrich

2,3-Diaminopyridin

Vetec™, reagent grade, 94%

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About This Item

Empirische Formel (Hill-System):
C5H7N3
CAS-Nummer:
452-58-4
Molekulargewicht:
109.13
Beilstein:
109869
EG-Nummer:
207-200-9
MDL-Nummer:
MFCD00006319
UNSPSC-Code:
12352100
PubChem Substanz-ID:
329830026

Qualität

reagent grade

Produktlinie

Vetec™

Assay

94%

mp (Schmelzpunkt)

110-115 °C (lit.)

SMILES String

Nc1cccnc1N

InChI

1S/C5H7N3/c6-4-2-1-3-8-5(4)7/h1-3H,6H2,(H2,7,8)

InChIKey

ZZYXNRREDYWPLN-UHFFFAOYSA-N

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Rechtliche Hinweise

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

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Scott D Kuduk et al.
Journal of medicinal chemistry, 47(26), 6439-6442 (2004-12-14)
Bradykinin B1 receptor antagonists embody a potentially novel approach for the treatment of chronic pain and inflammation. A series of 2,3-diaminopyridine B1 antagonists was optimized to have sub-nanomolar affinity and good pharmacokinetic properties. Lead compounds were shown to exhibit good
Xiangyang Shi et al.
Electrophoresis, 26(15), 2949-2959 (2005-07-05)
Generation 2 to generation 5 poly(amidoamine) (PAMAM) dendrimers having different terminal functionalities were analyzed by capillary electrophoresis (CE). Polyacrylamide gel electrophoresis was also used to assess the composition of the individual generations for comparison with the CE results. Separation of
Nessreen A Al-Hashimi
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(8-9), 2181-2184 (2004-07-14)
The charge-transfer interaction of 2,3-diaminopyridine (DAPY) and iodine has been investigated spectrophotometrically in the solvents chloroform and dichloromethane at room temperature. The results indicate the formation of 1:2 charge-transfer complex in each solvent with the observation of the two characteristic
Dong-Mei Feng et al.
Bioorganic & medicinal chemistry letters, 15(9), 2385-2388 (2005-04-20)
A novel class of 2,3-diaminopyridine bradykinin B1 receptor antagonists is disclosed. Structure-activity relationship studies (SARs) that led to compounds with significantly improved potency and pharmacokinetic properties relative to the lead compound are described.
Fengli Yu et al.
Talanta, 78(4-5), 1395-1400 (2009-04-14)
A new voltammetric enzyme-linked immunoassay system using the electrochemical substrate 2,3-diaminopyridine (DAP) and horseradish peroxidase (HRP) system has been developed. DAP is oxidized with H2O2 catalyzed by HRP, and the resulting electroactive product produces a sensitive voltammetric peak at potential
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