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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(3H)-Benzoxazolone, 5-amino-

Nc1ccc2c(c1)[nH]c(=O)o2 Request for Quotation
Chemical Name: 2(3H)-Benzoxazolone, 5-amino-
CAS Number: 14733-77-8
Product Number: AG001EU0(AGN-PC-0JKJ2X)
Synonyms:
MDL No:
Molecular Formula: C7H6N2O2
Molecular Weight: 150.1347

Identification/Properties

Computed Properties
Molecular Weight:
150.137g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
150.043g/mol
Monoisotopic Mass:
150.043g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
183
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Aminobenzo[d]oxazol-2(3H)-one, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and functional materials. Its ability to undergo diverse chemical transformations makes it a valuable intermediate in organic synthesis.In chemical synthesis, $name$ is commonly employed as a nucleophilic reagent due to the presence of the amino group, which enables it to participate in a range of reactions such as nucleophilic substitution, condensation, and cyclization. The oxazolone ring structure provides stability and enhances the compound's compatibility in various reaction conditions.Additionally, the presence of the benzene ring in the molecular structure of $name$ offers opportunities for further functionalization through aromatic substitution reactions, enabling the incorporation of additional functional groups into the molecule. This flexibility allows chemists to tailor the compound's properties for specific applications in drug discovery, material science, and other research fields.Overall, the strategic use of 5-Aminobenzo[d]oxazol-2(3H)-one in chemical synthesis allows for the efficient construction of complex molecules with desired characteristics, making it a valuable tool for organic chemists seeking to explore new synthetic pathways and develop innovative compounds.