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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, 7-fluoro-2,3-dihydro-

Fc1ccc2c(c1)OCCC2=O Request for Quotation
Chemical Name: 4H-1-Benzopyran-4-one, 7-fluoro-2,3-dihydro-
CAS Number: 113209-68-0
Product Number: AG003NFC(AGN-PC-0029SW)
Synonyms:
MDL No: MFCD06202344
Molecular Formula: C9H7FO2
Molecular Weight: 166.1491

Identification/Properties

Properties
MP:
53 °C
BP:
281.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
166.151g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
166.043g/mol
Monoisotopic Mass:
166.043g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
193
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Fluorochroman-4-one is a versatile compound widely used in chemical synthesis due to its unique properties. As a key building block in organic chemistry, it serves as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its ability to participate in a range of reactions, including nucleophilic substitutions, reductions, and cyclizations, makes it a valuable tool for forming complex molecular structures. Additionally, its fluorine atom imparts distinct reactivity and can be leveraged for further functionalization strategies in the creation of novel compounds. In summary, 7-Fluorochroman-4-one plays a crucial role in the synthesis of diverse chemical substances, demonstrating its significance in the realm of chemical research and development.