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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-Pyridinecarboxylic acid, 2-formyl-, methyl ester

COC(=O)c1ccnc(c1)C=O Request for Quotation
Chemical Name: 4-Pyridinecarboxylic acid, 2-formyl-, methyl ester
CAS Number: 125104-34-9
Product Number: AG000N7E(AGN-PC-02JGT5)
Synonyms:
MDL No:
Molecular Formula: C8H7NO3
Molecular Weight: 165.1461

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
165.148g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
165.043g/mol
Monoisotopic Mass:
165.043g/mol
Topological Polar Surface Area:
56.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
181
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-formylisonicotinate is a valuable compound widely used in chemical synthesis, particularly in the field of organic chemistry. This versatile molecule serves as a key building block in various synthetic reactions, offering a range of applications for the creation of new compounds.One notable application of Methyl 2-formylisonicotinate is its role as a precursor in the synthesis of pharmaceutical intermediates. Its functional groups and structural properties make it an ideal starting material for the construction of complex molecules with therapeutic potential. By incorporating Methyl 2-formylisonicotinate into synthetic pathways, chemists can efficiently access novel drug candidates and essential compounds for biological research.Additionally, this compound is utilized in the preparation of specialty chemicals and agrochemicals. Its unique chemical structure allows for the modification of its core framework, enabling the synthesis of tailored products with specific properties and functions. Through strategic transformations, Methyl 2-formylisonicotinate contributes to the development of innovative materials and formulations for various industrial applications.Furthermore, Methyl 2-formylisonicotinate plays a crucial role in academic research and chemical discovery. Its reactivity and compatibility with diverse reaction conditions make it a valuable tool for investigating new chemical transformations and exploring synthetic methodologies. Scientists leverage the versatility of this compound to advance knowledge in organic chemistry and expand the possibilities of molecular design.In conclusion, Methyl 2-formylisonicotinate stands as a vital component in chemical synthesis, offering a multitude of applications in pharmaceutical, industrial, and academic settings. Its contributions to the creation of novel compounds and the advancement of synthetic methodologies highlight its significance in the realm of organic chemistry.