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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-Oxazolecarboxaldehyde, 2,5-dimethyl-

O=Cc1nc(oc1C)C Request for Quotation
Chemical Name: 4-Oxazolecarboxaldehyde, 2,5-dimethyl-
CAS Number: 92901-88-7
Product Number: AG006KCQ(AGN-PC-0M0OMO)
Synonyms:
MDL No:
Molecular Formula: C6H7NO2
Molecular Weight: 125.1253

Identification/Properties

Properties
BP:
197.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
125.127g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
125.048g/mol
Monoisotopic Mass:
125.048g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
116
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:
Warning
UN#:
N/A
Hazard Statements:
H319
Precautionary Statements:
P337+P313-P305+P351+P338-P264-P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Dimethyloxazole-4-carbaldehyde is a versatile chemical compound commonly used in chemical synthesis applications. This aldehyde compound serves as a valuable building block in the creation of various organic compounds due to its reactivity and unique structural properties. In organic synthesis, 2,5-Dimethyloxazole-4-carbaldehyde can be utilized as a key intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals.One of the primary applications of 2,5-Dimethyloxazole-4-carbaldehyde is in the synthesis of heterocyclic compounds. By reacting this compound with different reagents and catalysts, chemists can produce a wide range of biologically active molecules with diverse functionalities. The presence of the oxazole and aldehyde functional groups in 2,5-Dimethyloxazole-4-carbaldehyde allows for the formation of complex structures through various chemical transformations.Additionally, 2,5-Dimethyloxazole-4-carbaldehyde is commonly used in the preparation of fluorescent dyes and imaging agents. Its ability to participate in condensation reactions and form stable adducts makes it a valuable component in the creation of fluorescent probes for biological imaging and detection purposes. The unique combination of fluorescence properties and chemical reactivity of this compound makes it a preferred choice in the development of novel imaging tools for scientific research and diagnostic applications.