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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)-

Methanone, phenylpyridinyl-, oxime

ON=C(c1ccccn1)c1ccccc1 Request for Quotation
Chemical Name: Methanone, phenylpyridinyl-, oxime
CAS Number: 1826-28-4
Product Number: AG00240U(AGN-PC-0O564F)
Synonyms:
MDL No:
Molecular Formula: C12H10N2O
Molecular Weight: 198.2206

Identification/Properties

Properties
MP:
154-156 °C(lit.)
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
198.225g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
198.079g/mol
Monoisotopic Mass:
198.079g/mol
Topological Polar Surface Area:
45.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
222
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H318-H335
Precautionary Statements:
P261-P280-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Phenyl(pyridin-2-yl)methanone oxime is a versatile compound widely used in chemical synthesis. It serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure provides opportunities for selective functional group transformations, making it a valuable tool for organic chemists.In chemical synthesis, Phenyl(pyridin-2-yl)methanone oxime acts as a versatile intermediate, participating in a variety of reactions such as acylation, alkylation, and reduction. It can undergo nucleophilic addition reactions to form new C-N or C-O bonds, allowing for the introduction of different functional groups. This compound also serves as a protecting group for carbonyl compounds, enabling sequential reactions without unwanted side reactions. Additionally, its oxime functionality can be easily converted back to the carbonyl group, further expanding its synthetic utility.Overall, Phenyl(pyridin-2-yl)methanone oxime plays a crucial role in the construction of complex organic molecules and is a valuable tool for chemists involved in medicinal chemistry, material science, and drug discovery.