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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)-

3-Pyridinecarboxylic acid, 4-methyl-, methyl ester

Cc1ccncc1C(=O)OC Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 4-methyl-, methyl ester
CAS Number: 33402-75-4
Product Number: AG00BZHQ(AGN-PC-0NC3CU)
Synonyms:
MDL No: MFCD09258869
Molecular Formula: C8H9NO2
Molecular Weight: 151.1626

Identification/Properties

Properties
BP:
215.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
151.165g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
151.063g/mol
Monoisotopic Mass:
151.063g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
147
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 4-methylnicotinate is a valuable compound in chemical synthesis due to its versatile applications. This specialized chemical is commonly employed as a precursor in the synthesis of various pharmaceutical and agrochemical compounds. Through strategic chemical reactions, Methyl 4-methylnicotinate can be transformed into a range of derivatives with diverse properties and functionalities. Its unique structural features make it an ideal building block for the creation of novel organic molecules with potential biological activities. In the field of medicinal chemistry, Methyl 4-methylnicotinate serves as a key intermediate in the synthesis of drugs targeting specific biological pathways. Additionally, its use in agrochemical synthesis contributes to the development of crop protection solutions and plant growth regulators. By harnessing the chemical reactivity of Methyl 4-methylnicotinate, researchers can access a multitude of synthetic pathways to produce valuable compounds for various applications.