Chemistry:Lutidinic acid
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Names | |
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Preferred IUPAC name
Pyridine-2,4-dicarboxylic acid | |
Other names
2,4-Pyridinedicarboxylic acid
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Identifiers | |
3D model (JSmol)
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131631 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
EC Number |
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279731 | |
PubChem CID
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UNII | |
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Properties | |
C7H5NO4 | |
Molar mass | 167.120 g·mol−1 |
Melting point | 242–243 °C (468–469 °F; 515–516 K)[1] |
Hazards | |
GHS pictograms | |
GHS Signal word | Warning |
H315, H319, H335 | |
P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Tracking categories (test):
Lutidinic acid (pyridine-2,4-dicarboxylic acid) is an heterocyclic organic compound, more precisely a heteroaromatic. It belongs to the group of pyridine dicarboxylic acids and consists of a pyridine ring which carries two carboxy groups in the 2- and 4-position.[2][3]
References
- ↑ "Safety Data Sheet" (in DE). https://www.merckmillipore.com/INTERSHOP/web/WFS/Merck-DE-Site/de_DE/-/EUR/ShowDocument-File?ProductSKU=MDA_CHEM-821052&DocumentId=821052_SDS_DE_DE.PDF&DocumentType=MSD&Language=DE&Country=DE.
- ↑ Meyer, Hans; Tropsch, Hans (1914). "Über Derivate der Lutidinsäure und das αγ-Diaminopyridin". Monatshefte Für Chemie 35 (2): 189–206. doi:10.1007/BF01518123.
- ↑ Richard Wolffenstein: Die Pflanzenalkaloide, 3. Auflage, Berlin 1922, S. 67 ([1], p. 67, at Google Books)
Original source: https://en.wikipedia.org/wiki/Lutidinic acid.
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