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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)-

N-methyl-1,3-oxazol-2-amine

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Chemical Name: N-methyl-1,3-oxazol-2-amine
CAS Number: 99170-93-1
Product Number: AG0039JA(AGN-PC-02R8EJ)
Synonyms:
MDL No:
Molecular Formula: C4H6N2O
Molecular Weight: 98.1032

Identification/Properties

Computed Properties
Molecular Weight:
98.105g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
98.048g/mol
Monoisotopic Mass:
98.048g/mol
Topological Polar Surface Area:
38.1A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
57.7
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-methyl-2-oxazolamine is a versatile reagent commonly used in chemical synthesis. In organic chemistry, it is frequently employed as a amidating agent for the functionalization of various compounds. Its ability to introduce an amide group makes it a valuable tool for the synthesis of peptides, pharmaceuticals, and complex organic molecules. Additionally, N-methyl-2-oxazolamine can participate in coupling reactions to form C-N bonds, making it useful for building molecular structures with nitrogen-containing functional groups. Its high reactivity and selectivity in these processes make it a popular choice for chemists working in the field of organic synthesis.