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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)-

Oxazole, 4,5-dimethyl-

Cc1ocnc1C Request for Quotation
Chemical Name: Oxazole, 4,5-dimethyl-
CAS Number: 20662-83-3
Product Number: AG002ILJ(AGN-PC-0JKL7N)
Synonyms:
MDL No:
Molecular Formula: C5H7NO
Molecular Weight: 97.1152

Identification/Properties

Properties
BP:
117.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
97.117g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
97.053g/mol
Monoisotopic Mass:
97.053g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
65.1
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:
Danger
UN#:
1993
Hazard Statements:
H226
Precautionary Statements:
P210-P233-P240-P241+P242+P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,5-Dimethyloxazole is a vital component in chemical synthesis, serving as a key building block for various organic compounds. Due to its unique chemical structure, it is commonly employed in the creation of pharmaceuticals, agrochemicals, and fragrances. This versatile compound undergoes various reactions such as acylation, alkylation, and cyclization, enabling the production of complex molecules with diverse functionalities. In organic synthesis, 4,5-Dimethyloxazole acts as a nucleophilic reactant, participating in reactions to form new carbon-carbon or carbon-heteroatom bonds. Its reactivity and compatibility with a wide range of functional groups make it a valuable tool in the creation of intricate molecular structures with potential applications in the fields of medicine, agriculture, and perfumery.