2,6-Dichloropyridine-4-carboxylic acid - CAS 5398-44-7
Catalog: |
BB028434 |
Product Name: |
2,6-Dichloropyridine-4-carboxylic acid |
CAS: |
5398-44-7 |
Synonyms: |
2,6-dichloropyridine-4-carboxylic acid |
IUPAC Name: | 2,6-dichloropyridine-4-carboxylic acid |
Description: | 2,6-Dichloropyridine-4-carboxylic acid (CAS# 5398-44-7) is a derivative of isonicotinic acid (I821760). Treatment of oat cultivars using 2,6-dichloroisonicotinic acid results in an increased accumulation of avenathramide. 2,6-Dichloroisonicotinic acid is a well known inducer of plant resistance and induces the transcription of ZmNAC100 transcription factor. |
Molecular Weight: | 192.00 |
Molecular Formula: | C6H3Cl2NO2 |
Canonical SMILES: | C1=C(C=C(N=C1Cl)Cl)C(=O)O |
InChI: | InChI=1S/C6H3Cl2NO2/c7-4-1-3(6(10)11)2-5(8)9-4/h1-2H,(H,10,11) |
InChI Key: | SQSYNRCXIZHKAI-UHFFFAOYSA-N |
Boiling Point: | 437.8 °C at 760 mmHg |
Melting Point: | 210-211 °C |
Purity: | 95 % |
Density: | 1.612 g/cm3 |
Appearance: | White crystals |
MDL: | MFCD00234147 |
LogP: | 2.08660 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
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PMID | Publication Date | Title | Journal |
22835274 | 20121101 | Nitric oxide-mediated stress imprint in potato as an effect of exposure to a priming agent | Molecular plant-microbe interactions : MPMI |
22120123 | 20120501 | Fumonisin B1, a toxin produced by Fusarium verticillioides, modulates maize β-1,3-glucanase activities involved in defense response | Planta |
22483270 | 20120407 | Synthesis and antibacterial activity against ralstonia solanacearum for novel hydrazone derivatives containing a pyridine moiety | Chemistry Central journal |
22353606 | 20120221 | A rice transient assay system identifies a novel domain in NRR required for interaction with NH1/OsNPR1 and inhibition of NH1-mediated transcriptional activation | Plant methods |
22489201 | 20120101 | New synthetic pyridine derivate as potential elicitor in production of isoflavonoids and flavonoids in Trifolium pratense L. suspension culture | TheScientificWorldJournal |
Complexity: | 155 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 190.9540837 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 190.9540837 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 50.2 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.6 |
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