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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)-

9H-Fluorene, 2-bromo-7-iodo-

Brc1ccc2c(c1)Cc1c2ccc(c1)I Request for Quotation
Chemical Name: 9H-Fluorene, 2-bromo-7-iodo-
CAS Number: 123348-27-6
Product Number: AG000KEY(AGN-PC-000YHL)
Synonyms:
MDL No:
Molecular Formula: C13H8BrI
Molecular Weight: 371.0111

Identification/Properties

Computed Properties
Molecular Weight:
371.015g/mol
XLogP3:
4.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
369.885g/mol
Monoisotopic Mass:
369.885g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
243
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:
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


9H-Fluorene, 2-bromo-7-iodo- is a versatile compound widely used in chemical synthesis. This specific derivative of fluorene plays a crucial role in various organic reactions due to the unique properties it possesses. In chemical synthesis, 9H-Fluorene, 2-bromo-7-iodo- is often employed as a key building block for the synthesis of complex organic molecules. Its strategic placement of bromo and iodo groups allows for selective functionalization at these positions, enabling chemists to incorporate specific functional groups with precision.Furthermore, the presence of both bromine and iodine in this compound enhances its reactivity in cross-coupling reactions, making it an essential reagent for the formation of carbon-carbon and carbon-heteroatom bonds. This capability opens up a wide range of synthetic pathways, leading to the creation of diverse molecular structures with potential applications in pharmaceuticals, materials science, and other fields.Overall, 9H-Fluorene, 2-bromo-7-iodo- serves as a valuable tool in chemical synthesis, facilitating the construction of complex organic molecules with tailored functionalities through controlled and efficient reactions.