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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)-

2-bromo-1-ethenyl-4-fluorobenzene

C=Cc1ccc(cc1Br)F Request for Quotation
Chemical Name: 2-bromo-1-ethenyl-4-fluorobenzene
CAS Number: 1221684-51-0
Product Number: AG0016VD(AGN-PC-093FKS)
Synonyms:
MDL No:
Molecular Formula: C8H6BrF
Molecular Weight: 201.0356

Identification/Properties

Computed Properties
Molecular Weight:
201.038g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
199.964g/mol
Monoisotopic Mass:
199.964g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
124
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:
Danger
UN#:
1760
Hazard Statements:
H227-H315-H317-H318-H335
Precautionary Statements:
P210-P261-P264-P271-P272-P280-P302+P352-P304+P340-P305+P351+P338-P310-P332+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-4-fluoro-1-vinylbenzene, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound is commonly employed as a building block in the synthesis of various organic molecules and materials.One of the key applications of 2-Bromo-4-fluoro-1-vinylbenzene is its use as a precursor in the preparation of pharmaceutical compounds. By undergoing various chemical reactions, this compound can be transformed into more complex structures that exhibit important biological activities. Its vinylbenzene moiety allows for easy functionalization and modification, making it a valuable intermediate in drug discovery and development.Additionally, 2-Bromo-4-fluoro-1-vinylbenzene is utilized in the production of specialty polymers and materials. Its vinyl functionality enables polymerization reactions to occur, leading to the formation of polymers with specific properties and applications. This compound can be incorporated into polymer chains to impart desired characteristics such as thermal stability, chemical resistance, or optical properties.Moreover, 2-Bromo-4-fluoro-1-vinylbenzene serves as a useful reagent in organic synthesis for the construction of various carbon-carbon and carbon-heteroatom bonds. Its bromine and fluorine substituents can participate in a range of coupling and substitution reactions, allowing chemists to access structurally diverse compounds with relative ease.Overall, 2-Bromo-4-fluoro-1-vinylbenzene plays a crucial role in modern chemical synthesis as a versatile building block with diverse applications in the pharmaceutical, materials, and fine chemical industries. Its reactivity and compatibility with various reaction conditions make it a valuable tool for chemists seeking to create novel molecules and materials for a wide range of applications.