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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-(acetyloxy)-4-(bromomethyl)-

BrCc1cc(=O)oc2c1ccc(c2)OC(=O)C Request for Quotation
Chemical Name: 2H-1-Benzopyran-2-one, 7-(acetyloxy)-4-(bromomethyl)-
CAS Number: 2747-04-8
Product Number: AG003NCH(AGN-PC-0JNK23)
Synonyms:
MDL No:
Molecular Formula: C12H9BrO4
Molecular Weight: 297.10146

Identification/Properties

Properties
MP:
184-185°C
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
297.104g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
295.968g/mol
Monoisotopic Mass:
295.968g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
364
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Bromomethyl)-2-oxo-2H-chromen-7-yl acetate, commonly used in chemical synthesis, is a versatile compound that finds widespread application in organic chemistry. Its functional groups and structure make it an excellent building block in the creation of various organic molecules. This compound is particularly valued for its ability to act as a key intermediate in the synthesis of biologically active compounds, pharmaceuticals, and agrochemicals. Its unique arrangement of atoms allows for precise modifications and transformations, enabling chemists to create complex structures efficiently. Additionally, the presence of the bromine atom enhances its reactivity, making it a valuable tool in organic transformations such as nucleophilic substitutions and palladium-catalyzed coupling reactions. This compound's role in chemical synthesis extends to the creation of novel materials, dyes, and other specialty chemicals, showcasing its importance in the field of organic chemistry.