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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-Oxazolemethanol, 2-methyl-

Cc1nc(co1)CO Request for Quotation
Chemical Name: 4-Oxazolemethanol, 2-methyl-
CAS Number: 141567-53-5
Product Number: AG007ZAC(AGN-PC-0LQ1JO)
Synonyms:
MDL No:
Molecular Formula: C5H7NO2
Molecular Weight: 113.1146

Identification/Properties

Computed Properties
Molecular Weight:
113.116g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
113.048g/mol
Monoisotopic Mass:
113.048g/mol
Topological Polar Surface Area:
46.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
76.8
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2-Methyloxazol-4-yl)methanol, also known as $name$, is a versatile compound that finds wide applications in chemical synthesis. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a crucial intermediate in the synthesis of complex organic molecules.In organic chemistry, (2-Methyloxazol-4-yl)methanol is often utilized as a key starting material for the synthesis of heterocyclic compounds. It acts as a precursor for the construction of diverse chemical structures through functional group transformations and cyclization reactions. Its presence in a synthetic pathway can significantly facilitate the formation of important chemical bonds and enhance the efficiency of multistep syntheses.Furthermore, (2-Methyloxazol-4-yl)methanol exhibits versatile reactivity patterns that allow for the introduction of various functional groups at specific positions within a molecule. This selective reactivity makes it a valuable tool for chemists seeking to control the regioselectivity and stereochemistry of their target compounds. By leveraging the unique properties of this compound, researchers can access a wide array of structurally diverse molecules with tailored properties and functionalities.Overall, the application of (2-Methyloxazol-4-yl)methanol in chemical synthesis enables the efficient and precise construction of complex organic molecules with potential applications in pharmaceuticals, agrochemicals, and materials science. Scientists and synthetic chemists continue to explore its versatile chemistry and harness its synthetic utility in the pursuit of novel chemical entities and innovative solutions to challenges in drug discovery and materials design.