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  2. 5-O-methyl 3-O-(2-methylpropyl) 2,6-dimethyl-4-(2-nitrophenyl)pyridine-3,5-dicarboxylate

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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)-

5-O-methyl 3-O-(2-methylpropyl) 2,6-dimethyl-4-(2-nitrophenyl)pyridine-3,5-dicarboxylate

COC(=O)c1c(C)nc(c(c1c1ccccc1[N+](=O)[O-])C(=O)OCC(C)C)C Request for Quotation
Chemical Name: 5-O-methyl 3-O-(2-methylpropyl) 2,6-dimethyl-4-(2-nitrophenyl)pyridine-3,5-dicarboxylate
CAS Number: 103026-83-1
Product Number: AG00865S(AGN-PC-0N3LAE)
Synonyms:
MDL No:
Molecular Formula: C20H22N2O6
Molecular Weight: 386.3985

Identification/Properties

Computed Properties
Molecular Weight:
386.404g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
7
Exact Mass:
386.148g/mol
Monoisotopic Mass:
386.148g/mol
Topological Polar Surface Area:
111A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
576
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Isobutyl 5-methyl 2,6-dimethyl-4-(2-nitrophenyl)pyridine-3,5-dicarboxylate is a versatile compound commonly utilized in chemical synthesis processes. Its unique molecular structure makes it an ideal building block for the creation of various organic compounds. This compound is particularly valuable in the production of pharmaceutical intermediates and fine chemicals due to its reactivity and stability under various reaction conditions. Additionally, its nitrophenyl group provides a site for further functionalization, allowing for the synthesis of diverse derivatives with tailored properties. In the field of materials science, this compound is employed in the design and synthesis of novel polymers and catalysts. Its presence enhances the reactivity and selectivity of certain chemical reactions, making it a valuable tool for synthetic chemists seeking to develop new and innovative compounds.