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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)-

1H-Inden-1-one, 2,3-dihydro-5-(trifluoromethyl)-

O=C1CCc2c1ccc(c2)C(F)(F)F Request for Quotation
Chemical Name: 1H-Inden-1-one, 2,3-dihydro-5-(trifluoromethyl)-
CAS Number: 150969-56-5
Product Number: AG001MY8(AGN-PC-0NHZYZ)
Synonyms:
MDL No:
Molecular Formula: C10H7F3O
Molecular Weight: 200.1572

Identification/Properties

Properties
MP:
58 - 60°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
200.16g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
200.045g/mol
Monoisotopic Mass:
200.045g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
246
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#:
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

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Chemical Structure


5-(Trifluoromethyl)-2,3-dihydro-1H-inden-1-one is a versatile compound commonly employed in chemical synthesis due to its unique properties and reactivity. When used in organic synthesis, this compound serves as a valuable building block for the construction of various complex molecules. Its trifluoromethyl group enhances the compound's stability and influences its chemical behavior, making it a valuable tool in modern organic chemistry.In the field of medicinal chemistry, 5-(Trifluoromethyl)-2,3-dihydro-1H-inden-1-one has shown promise as a key intermediate in the synthesis of pharmaceuticals and bioactive compounds. The presence of the trifluoromethyl moiety can enhance the biological activity of the resulting molecules, making them potentially more effective as therapeutic agents. Additionally, this compound can be utilized in the synthesis of agrochemicals, dyes, and materials with specialized properties.Furthermore, in the development of new materials, 5-(Trifluoromethyl)-2,3-dihydro-1H-inden-1-one can be employed to introduce unique functional groups and structural motifs, allowing for the creation of novel materials with tailored properties. Its reactivity and compatibility with various synthetic methods make it a valuable tool for researchers seeking to design and optimize innovative materials for a wide range of applications.