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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-chloro-4,6-dimethoxy-

COc1cc(OC)nc(c1)Cl Request for Quotation
Chemical Name: Pyridine, 2-chloro-4,6-dimethoxy-
CAS Number: 108279-89-6
Product Number: AG00337Q(AGN-PC-0NCAD3)
Synonyms:
MDL No:
Molecular Formula: C7H8ClNO2
Molecular Weight: 173.5969

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
173.596g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
173.024g/mol
Monoisotopic Mass:
173.024g/mol
Topological Polar Surface Area:
31.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
123
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


2-Chloro-4,6-dimethoxypyridine, also known as $name$, serves as a versatile building block in chemical synthesis. This compound plays a crucial role in various reactions and transformations due to its unique chemical properties.One important application of 2-Chloro-4,6-dimethoxypyridine is in the synthesis of pharmaceutical intermediates. It can be used as a key starting material in the preparation of diverse pharmaceutical compounds, facilitating the formation of complex molecular structures with specific biological activities. Its presence in the synthesis pathway can enable the introduction of essential functional groups and structural motifs required for enhancing the efficacy and potency of the final drug product.Additionally, 2-Chloro-4,6-dimethoxypyridine is utilized in the production of agrochemicals. By incorporating this compound into the synthesis of agricultural products, novel pesticides or herbicides can be developed with enhanced efficiency and selectivity. The presence of the chloro and methoxy substituents in the pyridine ring imparts specific chemical reactivity to the molecule, allowing for targeted modifications and improvements in the performance of agrochemical formulations.Furthermore, in the field of material science, 2-Chloro-4,6-dimethoxypyridine finds applications in the design and fabrication of advanced materials. Its chemical structure can participate in cross-coupling reactions, functional group transformations, and other synthetic pathways that lead to the creation of functional materials with tailored properties. These materials can exhibit specific characteristics such as enhanced stability, conductivity, or optical properties, making them valuable for various industrial applications.Overall, the versatile nature of 2-Chloro-4,6-dimethoxypyridine makes it an indispensable tool in chemical synthesis, enabling the creation of diverse compounds and materials for pharmaceutical, agrochemical, and material science applications.