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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, 3-chloro-, 1-oxide

[O-][n+]1cccc(c1)Cl Request for Quotation
Chemical Name: Pyridine, 3-chloro-, 1-oxide
CAS Number: 1851-22-5
Product Number: AG0074LW(AGN-PC-047187)
Synonyms:
MDL No:
Molecular Formula: C5H4ClNO
Molecular Weight: 129.5444

Identification/Properties

Computed Properties
Molecular Weight:
129.543g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
128.998g/mol
Monoisotopic Mass:
128.998g/mol
Topological Polar Surface Area:
25.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
78.8
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:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Chloropyridine 1-oxide is a versatile compound used in various chemical synthesis processes. Due to its unique structure and reactivity, this compound finds applications in the synthesis of pharmaceuticals, agrochemicals, and organic intermediates. In organic synthesis, 3-Chloropyridine 1-oxide serves as a valuable building block for the production of complex molecules with specific functionalities. Its ability to undergo various chemical reactions, such as nucleophilic substitution, oxidation, and cyclization, makes it a vital component in the creation of diverse chemical compounds. Additionally, 3-Chloropyridine 1-oxide has been employed in the preparation of heterocyclic compounds, which are important in drug discovery and development. Overall, the use of 3-Chloropyridine 1-oxide in chemical synthesis showcases its significance in advancing modern organic chemistry and facilitating the creation of novel chemical entities.