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P42800

Sigma-Aldrich

2-Picolinic acid

ReagentPlus®, 99%

Synonym(s):

α-Picolinic acid, Pyridine-2-carboxylic acid

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About This Item

Empirical Formula (Hill Notation):
C6H5NO2
CAS Number:
98-98-6
Molecular Weight:
123.11
Beilstein/REAXYS Number:
109595
EC Number:
202-719-7
MDL number:
MFCD00006293
UNSPSC Code:
12352100
PubChem Substance ID:
24898523
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

200

product line

ReagentPlus®

assay

99%

form

crystals

reaction suitability

reagent type: catalyst
reagent type: ligand
reaction type: C-H Activation

mp

139-142 °C (lit.)

functional group

carboxylic acid

SMILES string

OC(=O)c1ccccn1

InChI

1S/C6H5NO2/c8-6(9)5-3-1-2-4-7-5/h1-4H,(H,8,9)

InChI key

SIOXPEMLGUPBBT-UHFFFAOYSA-N

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Show Differences

1 of 4

This Item
615757I175088.00614
2-Picolinic acid ReagentPlus®, 99%

P42800

2-Picolinic acid

2-Picolinic-d4 acid 98 atom % D

615757

2-Picolinic-d4 acid

Isonicotinic acid 99%

I17508

Isonicotinic acid

Pyridine-2,6-dicarboxylic acid for synthesis

8.00614

Pyridine-2,6-dicarboxylic acid

reaction suitability

reagent type: catalyst, reagent type: ligand
reaction type: C-H Activation

reaction suitability

-

reaction suitability

-

reaction suitability

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

mp

139-142 °C (lit.)

mp

139-142 °C

mp

≥300 °C (lit.)

mp

248-255 °C

form

crystals

form

solid

form

powder

form

powder

product line

ReagentPlus®

product line

-

product line

-

product line

-

Application

Chelate for alkaline earth metals.[1] Used to prepare picolinato ligated transition metal complexes.[2][3][4]

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H318

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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    Certificates of Analysis (COA)

    Lot/Batch Number
    WXBD5591V
    WXBD2677V
    WXBD1739V
    WXBD0326V
    WXBC8714V

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    Transition Met. Chem. (London), 19, 521-521 (1994)
    Orient. J. Chem., 9, 60-60 (1993)
    Monatshefte fur Chemie / Chemical Monthly, 125, 833-833 (1994)
    Lisheng Deng et al.
    Journal of medicinal chemistry, 54(13), 4721-4734 (2011-05-13)
    1-Deoxy-D-xylulose-5-phosphate reductoisomerase (DXR) is a novel target for developing new antibacterial (including antituberculosis) and antimalaria drugs. Forty-one lipophilic phosphonates, representing a new class of DXR inhibitors, were synthesized, among which 5-phenylpyridin-2-ylmethylphosphonic acid possesses the most activity against E. coli DXR
    Bhuvaneshwari Sundaram et al.
    BioFactors (Oxford, England), 38(1), 59-68 (2012-01-31)
    Chromium has been recognized as an essential trace element that plays an important role in carbohydrate metabolism. However, the molecular mechanisms involved in its action are not clear. This study was undertaken to understand the mechanism of chromium action in
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