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325228

Sigma-Aldrich

2-Methylpyridine-3-carboxylic acid

98%

Sinónimos:

2-Methylnicotinic acid, 2-Methylpyridine-3-carboxylic acid

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About This Item

Fórmula empírica (notación de Hill):
C7H7NO2
Número de CAS:
3222-56-8
Peso molecular:
137.14
Beilstein/REAXYS Number:
114333
MDL number:
MFCD00013449
UNSPSC Code:
12352100
PubChem Substance ID:
24859493
NACRES:
NA.22

assay

98%

mp

228-230 °C (dec.) (lit.)

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

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

Certificados de análisis (COA)

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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)
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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
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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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