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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)-

8-(4-aminophenyl)-2-morpholin-4-ylchromen-4-one

Nc1ccc(cc1)c1cccc2c1oc(cc2=O)N1CCOCC1 Request for Quotation
Chemical Name: 8-(4-aminophenyl)-2-morpholin-4-ylchromen-4-one
CAS Number: 942289-87-4
Product Number: AG0065KC(AGN-PC-04XEJ3)
Synonyms:
MDL No: MFCD11100185
Molecular Formula: C19H18N2O3
Molecular Weight: 322.3578

Identification/Properties

Computed Properties
Molecular Weight:
322.364g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
322.132g/mol
Monoisotopic Mass:
322.132g/mol
Topological Polar Surface Area:
64.8A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
493
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


LY294002, 4γ-NH2 is a versatile and potent chemical compound commonly employed in chemical synthesis procedures. Its unique structure and properties make it a valuable reagent for various applications in the field of organic chemistry.In chemical synthesis, LY294002, 4γ-NH2 is frequently utilized as a key building block for the creation of complex organic molecules. Its amino group enables selective functionalization and modification reactions, allowing chemists to strategically introduce desired functionalities into target compounds. This versatility makes LY294002, 4γ-NH2 an essential tool for synthesizing novel pharmaceuticals, agrochemicals, and materials with tailored properties.Furthermore, the presence of the 4γ substitution on the LY294002 scaffold enhances its reactivity and compatibility with a wide range of reaction conditions. This structural feature not only promotes efficient bond formation but also enables chemists to access diverse chemical space for exploring new synthetic pathways and strategies.Additionally, LY294002, 4γ-NH2 has demonstrated excellent stability and compatibility with different reaction partners, making it a reliable synthetic building block for generating structurally intricate molecules. Its successful integration into various synthetic protocols highlights its significance as a valuable reagent for advancing chemical synthesis strategies and achieving targeted molecular designs.