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:
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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
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)
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
Ignaz J Buerge et al.
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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
Naoki Takizawa et al.
Virology, 531, 126-140 (2019-03-16)
The influenza A virus genome consists of eight single-stranded negative-sense RNA segments. The noncoding regions located at the 3'- and 5'- ends of each segment are necessary for genome packaging, and the terminal coding regions are required to precisely bundle
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