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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)-

2H-1-Benzopyran-2-one, amino-

O=c1oc2ccccc2cc1N Request for Quotation
Chemical Name: 2H-1-Benzopyran-2-one, amino-
CAS Number: 1635-31-0
Product Number: AG001U5Y(AGN-PC-0JLBGZ)
Synonyms:
MDL No:
Molecular Formula: C9H7NO2
Molecular Weight: 161.1574

Identification/Properties

Properties
MP:
135-139℃ (lit.)
BP:
355.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
161.16g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
161.048g/mol
Monoisotopic Mass:
161.048g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
235
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:
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


3-Amino-2H-chromen-2-one, also known as acridin-9(10H)-one, is a versatile compound widely utilized in chemical synthesis for various applications. Its unique structure and reactivity make it a valuable building block in the creation of diverse organic compounds. One of the key applications of 3-Amino-2H-chromen-2-one is in the synthesis of heterocyclic compounds. This compound can undergo reactions with different electrophiles and nucleophiles to form fused heterocycles with nitrogen, oxygen, or sulfur atoms in the ring. These heterocyclic compounds have a wide range of biological activities and are used in the development of pharmaceuticals, agrochemicals, and materials.Furthermore, 3-Amino-2H-chromen-2-one can also be employed in the synthesis of fluorescent dyes and probes. By introducing specific functional groups to the chromenone scaffold, researchers can tailor the fluorescence properties of the resulting compounds for various applications in imaging, sensing, and detection.In addition to these applications, 3-Amino-2H-chromen-2-one has found utility in the preparation of complex molecules, natural product synthesis, and materials science. Its versatility and ease of functionalization make it a valuable precursor in organic chemistry, enabling the creation of diverse chemical structures with potential applications across different fields.