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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)-

[2-(4-methoxyphenyl)-1,3-oxazol-4-yl]methanamine

COc1ccc(cc1)c1occ(n1)CN Request for Quotation
Chemical Name: [2-(4-methoxyphenyl)-1,3-oxazol-4-yl]methanamine
CAS Number: 885272-87-7
Product Number: AG00472W(AGN-PC-05C72I)
Synonyms:
MDL No:
Molecular Formula: C11H12N2O2
Molecular Weight: 204.2252

Identification/Properties

Computed Properties
Molecular Weight:
204.229g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
204.09g/mol
Monoisotopic Mass:
204.09g/mol
Topological Polar Surface Area:
61.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
193
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 application of (2-(4-Methoxyphenyl)oxazol-4-yl)methanamine in chemical synthesis lies in its versatile nature as a building block for the synthesis of various organic compounds. This compound serves as a valuable intermediate in the creation of pharmaceuticals, agrochemicals, and materials due to its unique structural features and reactivity. By incorporating (2-(4-Methoxyphenyl)oxazol-4-yl)methanamine into synthetic pathways, chemists can access a wide range of functionalized molecules with tailored properties for diverse applications. Its presence enables the introduction of specific functional groups, enabling the modification of chemical structures to achieve desired characteristics and properties. Through strategic manipulation of its chemical reactivity, researchers can harness the potential of (2-(4-Methoxyphenyl)oxazol-4-yl)methanamine to drive innovation in the field of chemical synthesis.