Weight | 137.138 g/mol |
---|---|
Formula | C7H7NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
2-(pyridin-2-yl)acetic acid (13115-43-0, 54363-97-2)
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- Synthesis and antimycobacterial activity of [5-(pyridin-2-yl)-1,3,4-thiadiazol-2-ylthio]acetic acid arylidene-hydrazide derivatives. (Farmaco, 2001)
- Versatile synthetic approach to new bifunctional chelating agents tailor made for labeling with the fac-[M(CO)3]+ core (M = Tc, 99mTc, Re): synthesis, in vitro, and in vivo behavior of the model complex [M(APPA)(CO)3] (appa = [(5-amino-pentyl)-pyridin-2-yl-methyl-amino]-acetic acid) (Nuclear Medicine and Biology, 2003)
- Synthesis of (3-Carboxy-5-oxo-5H-[1]benzopyrano[2, 3-b]pyridin-2-yl)acetic Acid Derivatives, Potential Antiarthritic Agents (Chemical & Pharmaceutical Bulletin, 1986)
- The reaction of acetic acid 2selenoxo2Hpyridin1yl esters with benzynes: A convenient route to Benzo[b]seleno[2,3b]pyridines (Journal of Heterocyclic Chemistry, 2004)
- (E)-2-{4-[(Pyridin-2-yl)methylideneamino]phenyl}acetic acid (Acta Crystallographica Section E-structure Reports Online, 2012)
- 2-Phenylacetic acid3-{(E)-2-[(E)-pyridin-3-ylmethylidene]hydrazin-1-ylidenemethyl}pyridine (2/1) (Acta Crystallographica Section E-structure Reports Online, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=NC(=C1)CC(=O)O
-
InChIKeyBPSNETAIJADFTO-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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