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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:
109595
EC Number:
202-719-7
MDL number:
MFCD00006293
UNSPSC Code:
12352100
PubChem Substance ID:
24898523
NACRES:
NA.22

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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Application

Chelate for alkaline earth metals. Used to prepare picolinato ligated transition metal complexes.

Legal Information

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

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H318

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Orient. J. Chem., 9, 60-60 (1993)
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
Transition Met. Chem. (London), 19, 521-521 (1994)
Orient. J. Chem., 9, 43-43 (1993)
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