InChI key
NMMIHXMBOZYNET-UHFFFAOYSA-N
InChI
1S/C7H7NO2/c1-10-7(9)6-4-2-3-5-8-6/h2-5H,1H3
SMILES string
COC(=O)c1ccccn1
assay
99%
refractive index
n20/D 1.521 (lit.)
bp
95 °C/1 mmHg (lit.)
density
1.137 g/mL at 25 °C (lit.)
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
217.4 °F - closed cup
flash_point_c
103 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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
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)
Microwave-assisted organic synthesis of 3-substituted-imidazo [1, 5-a] pyridines.
Arvapalli VS, et al.
Tetrahedron Letters, 51(2), 284-286 (2010)
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.
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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