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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-bromo-2-(difluoromethoxy)-4-fluoro-

FC(Oc1cc(F)ccc1Br)F Request for Quotation
Chemical Name: Benzene,1-bromo-2-(difluoromethoxy)-4-fluoro-
CAS Number: 954235-83-7
Product Number: AG00IJ2H(AGN-PC-0W51GL)
Synonyms:
MDL No:
Molecular Formula: C7H4BrF3O
Molecular Weight: 241.0053

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
241.007g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
239.94g/mol
Monoisotopic Mass:
239.94g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
145
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Bromo-2-(difluoromethoxy)-4-fluorobenzene is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in organic chemistry, with applications in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. The presence of the bromo and fluoro substituents, coupled with the difluoromethoxy group, imparts distinct characteristics to the molecule, making it a valuable intermediate in the synthesis of complex organic molecules. Its ability to undergo diverse chemical transformations, such as nucleophilic aromatic substitution reactions, makes it a valuable tool for synthetic chemists looking to introduce specific functional groups or structural motifs into their target molecules. Overall, 1-Bromo-2-(difluoromethoxy)-4-fluorobenzene plays a crucial role in modern chemical synthesis, enabling the efficient construction of novel and industrially relevant compounds.