325228
2-Methylpyridine-3-carboxylic acid
98%
Synonym(s):
2-Methylnicotinic acid, 2-Methylpyridine-3-carboxylic acid
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About This Item
Empirical Formula (Hill Notation):
C7H7NO2
CAS Number:
Molecular Weight:
137.14
Beilstein/REAXYS Number:
114333
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
98%
mp
228-230 °C (dec.) (lit.)
functional group
carboxylic acid
SMILES string
Cc1ncccc1C(O)=O
InChI
1S/C7H7NO2/c1-5-6(7(9)10)3-2-4-8-5/h2-4H,1H3,(H,9,10)
InChI key
HNTZKNJGAFJMHQ-UHFFFAOYSA-N
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Application
2-Methylpyridine-3-carboxylic acid was used in synthesis of 1,8-dioxo-1,2,7,8-tetrahydro-2,7,10-triaza-anthracene-4,5-dicarbaldehydes (DOTTADs) and their imines. It was also used in synthesis of 7,7-dichloro-5,7-dihydro-thieno[3,4-b]pyridin-5-one.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Ashwini Kumar Ray et al.
Molecular and biochemical parasitology, 219, 42-51 (2017-11-28)
Selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) is a versatile sequence independent method to probe RNA structure in vivo and in vitro. It has so far been tried mainly with model organisms. We show that cells of Entamoeba histolytica
Andrea Arany et al.
Organic & biomolecular chemistry, 1(9), 1545-1551 (2003-08-21)
The interaction of Hantzsch pyridinecarboxylic acids with dialkylformamides and POCl3, followed by treatment with NH4OH yields 1,8-dioxo-1,2,7,8-tetrahydro-2,7,10-triazaanthracenes (DOTTADs), which have great potential as useful ligands for Group I and II metals and some transition metals. The corresponding Hantszch esters similarly
Preparation, X-ray structure and propylaminolysis of 7, 7-dichloro-5, 7-dihydro-thieno [3, 4-b] pyridin-5-one.
van Es T, et al.
J. Chem. Res. (M), 2007(6), 373-376 (2007)
Ignaz J Buerge et al.
Environmental science & technology, 53(10), 5725-5732 (2019-04-25)
Many pesticides show a pronounced biphasic degradation in soil, typically with a faster initial phase, followed by a slower decline. For chiral compounds, a biphasic decline of the total concentration may result from enantioselective degradation. In this study with the
Jamie Richards et al.
Molecular cell, 74(2), 284-295 (2019-03-11)
The diversity of mRNA lifetimes in bacterial cells is difficult to reconcile with the relaxed cleavage site specificity of RNase E, the endonuclease most important for governing mRNA degradation. This enzyme has generally been thought to locate cleavage sites by
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