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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 4-chloro-5-methylpyridine-2-carboxylate

COC(=O)c1ncc(c(c1)Cl)C Request for Quotation
Chemical Name: methyl 4-chloro-5-methylpyridine-2-carboxylate
CAS Number: 1104455-41-5
Product Number: AG007D7Q(AGN-PC-0ACAK3)
Synonyms:
MDL No:
Molecular Formula: C8H8ClNO2
Molecular Weight: 185.6076

Identification/Properties

Computed Properties
Molecular Weight:
185.607g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
185.024g/mol
Monoisotopic Mass:
185.024g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
174
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-chloro-5-methylpicolinate is a versatile chemical compound widely utilized in chemical synthesis for its unique reactivity and structural properties. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and materials due to its ability to participate in a range of key reactions.In chemical synthesis, Methyl 4-chloro-5-methylpicolinate acts as a crucial intermediate in the creation of heterocyclic compounds, which are essential structural motifs found in many biologically active molecules. Its presence allows for the introduction of both chloro and methyl substituents into the target molecules, enabling the fine-tuning of their properties and activities.Furthermore, Methyl 4-chloro-5-methylpicolinate is frequently employed in the construction of complex molecules through processes such as functional group transformation, cross-coupling reactions, and cyclization reactions. Its ease of manipulation and selective reactivity make it a valuable tool for chemists seeking to design and synthesize novel compounds with specific functions.Overall, the application of Methyl 4-chloro-5-methylpicolinate in chemical synthesis offers researchers and industry professionals a powerful means to access diverse chemical space and develop innovative products with tailored properties.