| Weight | 122.127 g/mol |
|---|---|
| Formula | C6H6N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Picolinamide (1452-77-3)
Score:
#25 in Medicinal chemistry
,
#5570 in Chemistry
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- Sigma-Aldrich - Picolinamide95.40 - 368.00 USD
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- A Practical Strategy for the Structural Diversification of Aliphatic Scaffolds through the PalladiumCatalyzed PicolinamideDirected Remote Functionalization of Unactivated C(sp3)H Bonds (Angewandte Chemie, 2011)
- Palladium-Catalyzed Picolinamide-Directed Alkylation of Unactivated C(sp3)H Bonds with Alkyl Iodides (Journal of the American Chemical Society, 2013)
- Efficient Alkyl Ether Synthesis via Palladium-Catalyzed, Picolinamide-Directed Alkoxylation of Unactivated C(sp3)H and C(sp2)H Bonds at Remote Positions (Journal of the American Chemical Society, 2012)
- Reusable directing groups [8-aminoquinoline, picolinamide, sulfoximine] in C(sp3)H bond activation: present and future (Tetrahedron, 2015)
- Recent Advances in the Treatment of Nuclear Wastes by the Use of Diamide and Picolinamide Extractants (Separation Science and Technology, 1995)
- Protection by picolinamide, a novel inhibitor of poly (ADP-ribose) synthetase, against both streptozotocin-induced depression of proinsulin synthesis and reduction of NAD content in pancreatic islets (Biochemical and Biophysical Research Communications, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=NC(=C1)C(=O)N
-
InChIKeyIBBMAWULFFBRKK-UHFFFAOYSA-N
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Picolinamide
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