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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)-

methyl 1-benzyl-2-oxo-3,4-dihydropyridine-5-carboxylate

COC(=O)C1=CN(C(=O)CC1)Cc1ccccc1 Request for Quotation
Chemical Name: methyl 1-benzyl-2-oxo-3,4-dihydropyridine-5-carboxylate
CAS Number: 156779-10-1
Product Number: AG001OZ2(AGN-PC-0N17MB)
Synonyms:
MDL No: MFCD18651682
Molecular Formula: C14H15NO3
Molecular Weight: 245.2738

Identification/Properties

Properties
Storage:
Room Temperature;Keep in dry area;
Computed Properties
Molecular Weight:
245.278g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
245.105g/mol
Monoisotopic Mass:
245.105g/mol
Topological Polar Surface Area:
46.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
356
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:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 1-Benzyl-2-oxo-1,2,3,4-tetrahydropyridine-5-carboxylate is a versatile compound commonly used in chemical synthesis due to its unique structural features and reactivity. This compound serves as a valuable building block in organic chemistry, allowing for the synthesis of various complex molecules and drug candidates through strategic modifications and transformations.In chemical synthesis, Methyl 1-Benzyl-2-oxo-1,2,3,4-tetrahydropyridine-5-carboxylate acts as a key intermediate that can undergo different types of reactions, such as nucleophilic additions, acylations, and reductions, to introduce new functional groups or generate intricate molecular structures. Its carbonyl group enables it to participate in important organic transformations, leading to the formation of diverse chemical compounds with potential biological activities.Moreover, the benzyl and methyl ester moieties in Methyl 1-Benzyl-2-oxo-1,2,3,4-tetrahydropyridine-5-carboxylate provide stability and flexibility for further derivatization, making it a valuable precursor in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. By carefully designing synthetic routes and utilizing the reactivity of this compound, chemists can access novel molecules with tailored properties and functionalities for various research and industrial applications.