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Sigma-Aldrich

Methyl picolinate

99%

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Empirical Formula (Hill Notation):
C7H7NO2
CAS Number:
Molecular Weight:
137.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

refractive index

n20/D 1.521 (lit.)

bp

95 °C/1 mmHg (lit.)

density

1.137 g/mL at 25 °C (lit.)

SMILES string

COC(=O)c1ccccn1

InChI

1S/C7H7NO2/c1-10-7(9)6-4-2-3-5-8-6/h2-5H,1H3

InChI key

NMMIHXMBOZYNET-UHFFFAOYSA-N

General description

Methyl picolinate (MP) exists in two conformers i.e s-trans and s-cis. Molecular structure of these forms has been investigated by gas electron diffraction.

Application

Methyl picolinate may be used in the synthesis of:
  • 3-substituted-imidazo[1,5-α]pyridines
  • N-benzylpicolinamide
  • 3-phenylsubstituted imidazo[1,5-α]pyridines
  • pyrimine
  • 4,6-dipyridylpyrimidine

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

217.4 °F

Flash Point(C)

103 °C

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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Structure determination of methyl nicotinate and methyl picolinate by gas electron diffraction combined with ab initio calculations.
Kiyono H, et al.
The Journal of Physical Chemistry A, 102(8), 1405-1411 (1998)
Peter J Steel
Molecules (Basel, Switzerland), 9(6), 440-448 (2007-11-17)
The syntheses of representative examples of five classes of new heterocyclic ligands are described. These include N,N'-chelating bis-heterocycles, binucleating ligands, cyclometallated compounds, chiral ligands and a family of polyheteroaryl-linked arenes.
Microwave-assisted organic synthesis of 3-substituted-imidazo [1, 5-a] pyridines.
Arvapalli VS, et al.
Tetrahedron Letters, 51(2), 284-286 (2010)
Mariétou F Paye et al.
Analytical biochemistry, 549, 80-90 (2018-03-20)
Research involving α/β hydrolases, including α-amino acid ester hydrolase and cocaine esterase, has been limited by the lack of an online high throughput screening assay. The development of a high throughput screening assay capable of detecting α/β hydrolase activity toward
Isolation, Characterization, and Synthesis of Pyrimine, an Iron (II)-Binding Agent from Pseudomonas GH*.
Shiman R and Neilands JB.
Biochemistry, 4(10), 2233-2236 (1965)

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