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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)-

1-(6-Chloropyridin-2-yl)ethanone

Clc1cccc(n1)C(=O)C Request for Quotation
Chemical Name: 1-(6-Chloropyridin-2-yl)ethanone
CAS Number: 152356-57-5
Product Number: AG00APBD(AGN-PC-00BZES)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO
Molecular Weight: 155.5816

Identification/Properties

Computed Properties
Molecular Weight:
155.581g/mol
XLogP3:
1.8
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:
138
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(6-Chloropyridin-2-yl)ethanone is a versatile compound that plays a crucial role in chemical synthesis. This compound serves as a key building block in the creation of various complex organic molecules, particularly in the pharmaceutical and agrochemical industries. Its unique structure and reactivity make it a valuable intermediate in the synthesis of biologically active compounds and functional materials. By incorporating 1-(6-Chloropyridin-2-yl)ethanone into synthetic pathways, chemists can efficiently access a wide range of structurally diverse molecules with potential applications in drug discovery, materials science, and other fields. This compound's ability to participate in diverse chemical reactions, including cross-coupling reactions and functional group transformations, underscores its significance as a versatile tool in modern organic synthesis strategies.