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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)-

4H-1-Benzopyran-4-one, 6-fluoro-

Fc1ccc2c(c1)c(=O)cco2 Request for Quotation
Chemical Name: 4H-1-Benzopyran-4-one, 6-fluoro-
CAS Number: 105300-38-7
Product Number: AG007F4W(AGN-PC-0JUYTO)
Synonyms:
MDL No:
Molecular Formula: C9H5FO2
Molecular Weight: 164.1332

Identification/Properties

Computed Properties
Molecular Weight:
164.135g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
164.027g/mol
Monoisotopic Mass:
164.027g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
225
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


6-Fluoro-4H-chromen-4-one is a versatile compound that finds wide application in chemical synthesis. This compound serves as a key building block in the creation of various bioactive molecules and pharmaceuticals due to its unique structure and reactivity. In synthetic organic chemistry, 6-Fluoro-4H-chromen-4-one can participate in a range of reactions such as nucleophilic substitution, Friedel-Crafts acylation, and Michael addition reactions. By functionalizing the fluoro group or modifying the chromenone ring system, chemists can access a plethora of structurally diverse compounds with potential biological activities. The addition of 6-Fluoro-4H-chromen-4-one in chemical syntheses offers a valuable tool for designing and developing new molecules with enhanced properties and functionalities for various applications in medicinal chemistry and material science.