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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-methyl-

Cc1ccc2c(c1)oc(=O)cc2 Request for Quotation
Chemical Name: 2H-1-Benzopyran-2-one, 7-methyl-
CAS Number: 2445-83-2
Product Number: AG003NGK(AGN-PC-0JKDA6)
Synonyms:
MDL No:
Molecular Formula: C10H8O2
Molecular Weight: 160.1693

Identification/Properties

Properties
MP:
128-130 °C(lit.)
BP:
313.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5300 (estimate)

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

Request for Quotation

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Chemical Structure


7-Methyl-2H-chromen-2-one is a versatile compound widely utilized in chemical synthesis processes due to its unique properties and reactivity. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, 7-Methyl-2H-chromen-2-one can be employed as a key intermediate in the production of complex organic molecules. Its rich chemistry allows for the facile modification of its structure through functional group transformations, making it a valuable precursor in the construction of diverse chemical scaffolds.Additionally, the presence of a chromenone moiety in 7-Methyl-2H-chromen-2-one offers opportunities for the development of novel therapeutic agents. Chemists can leverage this structure to design molecules with potential biological activities, such as anti-inflammatory, antimicrobial, or antioxidant properties.Overall, the strategic incorporation of 7-Methyl-2H-chromen-2-one in chemical synthesis not only enables the efficient generation of target molecules but also opens up avenues for the discovery of new compounds with significant industrial and pharmaceutical applications.