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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, 2-(bromomethyl)-1-fluoro-4-methoxy-

COc1ccc(c(c1)CBr)F Request for Quotation
Chemical Name: Benzene, 2-(bromomethyl)-1-fluoro-4-methoxy-
CAS Number: 91319-42-5
Product Number: AG00IGL6(AGN-PC-03HAEI)
Synonyms:
MDL No:
Molecular Formula: C8H8BrFO
Molecular Weight: 219.0509

Identification/Properties

Computed Properties
Molecular Weight:
219.053g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
217.974g/mol
Monoisotopic Mass:
217.974g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
121
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#:
1759
Hazard Statements:
H302-H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Bromomethyl)-1-fluoro-4-methoxybenzene is a versatile compound that finds valuable application in chemical synthesis. This compound, with its unique structure and reactivity, serves as a key building block for the construction of various organic molecules. In particular, it is often utilized in the synthesis of pharmaceuticals, agrochemicals, and materials due to its ability to introduce specific functional groups into target molecules.One important application of 2-(Bromomethyl)-1-fluoro-4-methoxybenzene is as a precursor in the synthesis of biologically active compounds. By incorporating this compound into chemical reactions, chemists can modify the structure of molecules to enhance their pharmacological properties or biological activities. This compound serves as an essential intermediate in the production of pharmaceutical agents, enabling the creation of new drug candidates or the optimization of existing medications.Furthermore, in the field of agrochemicals, 2-(Bromomethyl)-1-fluoro-4-methoxybenzene plays a crucial role in the development of crop protection products. Its incorporation into synthetic pathways allows for the tailoring of pesticides, herbicides, and fungicides with improved efficacy and specificity. By leveraging the reactivity of this compound, chemists can design novel active ingredients that target particular pests or weeds while minimizing environmental impact.Moreover, in materials science, the use of 2-(Bromomethyl)-1-fluoro-4-methoxybenzene enables the creation of functional polymers and specialty chemicals. This compound can be employed to functionalize polymers, coatings, and surfactants, imparting them with desired properties such as adhesion, durability, or electrical conductivity. Through strategic incorporation of this compound into material synthesis, researchers can develop innovative materials for diverse applications ranging from electronics to personal care products.