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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)-

3-chloro-6-methoxypyridine-2-carbaldehyde

COc1ccc(c(n1)C=O)Cl Request for Quotation
Chemical Name: 3-chloro-6-methoxypyridine-2-carbaldehyde
CAS Number: 1060810-35-6
Product Number: AG00HARH(AGN-PC-093FJJ)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO2
Molecular Weight: 171.5810

Identification/Properties

Computed Properties
Molecular Weight:
171.58g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
171.009g/mol
Monoisotopic Mass:
171.009g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
142
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-Chloro-6-methoxypicolinaldehyde, a versatile chemical reagent in organic synthesis, plays a crucial role in various reactions due to its unique properties. This compound is commonly used as a key building block for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to undergo diverse transformation reactions such as nucleophilic substitutions, condensation reactions, and cyclizations makes it a valuable intermediate in the production of advanced chemical compounds. In particular, it is frequently employed in the preparation of heterocyclic structures, which are essential components in a wide range of products.Moreover, 3-Chloro-6-methoxypicolinaldehyde exhibits excellent reactivity towards a variety of nucleophiles and electrophiles, allowing for the introduction of various functional groups with high selectivity. This enables chemists to tailor the chemical structure of the final product according to specific requirements.Furthermore, its unique molecular structure and distinct reactivity make 3-Chloro-6-methoxypicolinaldehyde a valuable tool for the development of novel chemical entities with potential applications in drug discovery, materials science, and other fields of research.