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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)-

(5-(3-chlorophenyl)oxazole-4-yl)methanol

OCc1ncoc1c1cccc(c1)Cl Request for Quotation
Chemical Name: (5-(3-chlorophenyl)oxazole-4-yl)methanol
CAS Number: 1020252-88-3
Product Number: AG0006CG(AGN-PC-07XTRX)
Synonyms:
MDL No:
Molecular Formula: C10H8ClNO2
Molecular Weight: 209.6290

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
209.629g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
209.024g/mol
Monoisotopic Mass:
209.024g/mol
Topological Polar Surface Area:
46.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
191
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#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (5-(3-Chlorophenyl)oxazol-4-yl)methanol, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. It serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. With its unique structure, $name$ offers a wide range of synthetic pathways and functional group transformations, making it a valuable tool for medicinal chemistry, organic synthesis, and materials science. Its strategic placement of a chlorophenyl oxazole moiety coupled with a hydroxyl group provides opportunities for diversification through selective chemical reactions, enabling efficient access to structurally complex molecules with desired properties. In the hands of skilled chemists, $name$ can be manipulated and tailored to design novel compounds with enhanced biological activities, improved pharmacokinetic profiles, and unique structural features for various applications in drug discovery and chemical research.