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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)-

Benzene, 1-(2-bromoethyl)-2-fluoro-

BrCCc1ccccc1F Request for Quotation
Chemical Name: Benzene, 1-(2-bromoethyl)-2-fluoro-
CAS Number: 91319-54-9
Product Number: AG003CTG(AGN-PC-0KKLF2)
Synonyms:
MDL No:
Molecular Formula: C8H8BrF
Molecular Weight: 203.0515

Identification/Properties

Properties
BP:
205.1°C at 760 mmHg
Storage:
Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
203.054g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
201.979g/mol
Monoisotopic Mass:
201.979g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
95.3
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-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(2-Bromoethyl)-2-fluorobenzene, also known as $name$, is a versatile chemical compound widely used in organic synthesis. Its application in chemical synthesis revolves around its unique structural properties which make it a valuable building block for the creation of various functional molecules. One of the key uses of 1-(2-Bromoethyl)-2-fluorobenzene is as a precursor in the preparation of fluorinated organic compounds. The presence of the bromoethyl and fluoro substituents on the benzene ring allows for selective functionalization reactions, enabling the introduction of diverse functional groups onto the aromatic system. This versatility is particularly useful in the design and synthesis of pharmaceuticals, agrochemicals, and advanced materials.Furthermore, the presence of both the bromoethyl and fluoro groups enhances the reactivity of 1-(2-Bromoethyl)-2-fluorobenzene in cross-coupling reactions, such as Suzuki and Heck reactions. These transformations play a crucial role in the construction of complex organic molecules by forming new carbon-carbon and carbon-heteroatom bonds. The resulting products can exhibit enhanced properties or functionalities compared to their precursors.Overall, the strategic incorporation of 1-(2-Bromoethyl)-2-fluorobenzene into synthetic routes enables chemists to access a wide range of structurally diverse compounds with potential applications in medicinal chemistry, materials science, and more. Its utility as a key intermediate highlights its significance in modern organic synthesis strategies.