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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)-

Pyridine, 2-methoxy-4-methyl-

COc1nccc(c1)C Request for Quotation
Chemical Name: Pyridine, 2-methoxy-4-methyl-
CAS Number: 100848-70-2
Product Number: AG00030Q(AGN-PC-000RCT)
Synonyms:
MDL No:
Molecular Formula: C7H9NO
Molecular Weight: 123.1525

Identification/Properties

Computed Properties
Molecular Weight:
123.155g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
123.068g/mol
Monoisotopic Mass:
123.068g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
85
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#:
1993
Hazard Statements:
H226-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methoxy-4-methylpyridine, also known as Methyl 2-methoxypyridine-4-carboxylate, is a versatile compound frequently used in chemical synthesis. This molecule plays a key role in various reactions as a building block for the synthesis of more complex organic compounds. In organic synthesis, 2-Methoxy-4-methylpyridine is commonly employed as a nucleophile in nucleophilic substitution reactions. It can participate in reactions such as Mannich-type condensations and Suzuki-Miyaura cross-coupling reactions, where its unique structure allows for the formation of new carbon-carbon and carbon-heteroatom bonds.Additionally, 2-Methoxy-4-methylpyridine can be utilized as a ligand in transition metal-catalyzed reactions. Its nitrogen atom can coordinate with metals, enhancing catalytic activity in processes like Heck coupling and C-H activation reactions. This compound's ability to stabilize metal centers and facilitate electron transfer makes it a valuable tool in modern synthetic chemistry.Overall, the application of 2-Methoxy-4-methylpyridine in chemical synthesis highlights its importance as a versatile reagent for building complex organic molecules and facilitating catalytic transformations.