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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)-

4-Pyridinecarboxaldehyde, 2-chloro-6-methyl-

O=Cc1cc(C)nc(c1)Cl Request for Quotation
Chemical Name: 4-Pyridinecarboxaldehyde, 2-chloro-6-methyl-
CAS Number: 479613-16-6
Product Number: AG00D8EY(AGN-PC-0KKP7M)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO
Molecular Weight: 155.5816

Identification/Properties

Properties
BP:
250.4 °C at 760 mmHg
Storage:
2-8℃;Inert atmosphere;
Computed Properties
Molecular Weight:
155.581g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
155.014g/mol
Monoisotopic Mass:
155.014g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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#:
-
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-6-methylisonicotinaldehyde, also known as $name$, serves as a valuable building block in chemical synthesis. This compound is commonly utilized as a key intermediate in the production of various pharmaceuticals and agrochemicals due to its versatile reactivity and functionality. Its unique structure allows for precise modifications and manipulations during synthetic processes, enabling the creation of complex molecules with specific properties and functions. In organic synthesis, 2-Chloro-6-methylisonicotinaldehyde plays a crucial role in the construction of heterocyclic compounds, which are vital components in drug discovery and material science applications. Its ability to undergo selective reactions makes it a valuable tool for chemists in developing new chemical entities with targeted biological activities. By incorporating 2-Chloro-6-methylisonicotinaldehyde into synthetic routes, researchers can access a wide range of structurally diverse compounds with potential pharmacological and commercial significance.