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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, 7-(ethylamino)-4,6-dimethyl-

CCNc1cc2oc(=O)cc(c2cc1C)C Request for Quotation
Chemical Name: 2H-1-Benzopyran-2-one, 7-(ethylamino)-4,6-dimethyl-
CAS Number: 26078-25-1
Product Number: AG002RLS(AGN-PC-0JM27L)
Synonyms:
MDL No:
Molecular Formula: C13H15NO2
Molecular Weight: 217.2637

Identification/Properties

Properties
MP:
168-170℃
Form:
Solid
Computed Properties
Molecular Weight:
217.268g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
217.11g/mol
Monoisotopic Mass:
217.11g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
311
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-(Ethylamino)-4,6-dimethyl-2H-chromen-2-one is a versatile compound that finds widespread application in chemical synthesis. Due to its unique molecular structure, this compound serves as a valuable building block for the creation of various derivatives and pharmaceutical intermediates. In organic synthesis, it can undergo various reactions such as alkylation, acylation, and oxidation to yield new compounds with diverse chemical properties. Additionally, its chromenone scaffold offers opportunities for modification, making it a valuable tool for the design and synthesis of novel molecules with potential biological activities.