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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, 4-bromo-2-iodo-1-methoxy-

COc1ccc(cc1I)Br Request for Quotation
Chemical Name: Benzene, 4-bromo-2-iodo-1-methoxy-
CAS Number: 98273-59-7
Product Number: AG00IK22(AGN-PC-0NDV6Y)
Synonyms:
MDL No:
Molecular Formula: C7H6BrIO
Molecular Weight: 312.9304

Identification/Properties

Computed Properties
Molecular Weight:
312.932g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
311.865g/mol
Monoisotopic Mass:
311.865g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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


4-Bromo-2-iodo-1-methoxybenzene, also known as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique structural properties. This compound serves as a crucial building block in the creation of various complex organic molecules, making it a valuable tool in the field of medicinal chemistry and materials science. 
One of the key applications of 4-Bromo-2-iodo-1-methoxybenzene is in the synthesis of pharmaceutical intermediates. Its ability to undergo various functional group transformations enables the efficient construction of biologically active compounds. Additionally, this compound is utilized in the preparation of agrochemicals and dyes, highlighting its significance in the development of innovative products across different industries. The presence of both bromine and iodine groups in the molecule provides diverse reactivity pathways, allowing for the synthesis of a wide range of chemical entities with tailored properties.
In conclusion, 4-Bromo-2-iodo-1-methoxybenzene plays a crucial role in chemical synthesis, offering a versatile platform for the creation of diverse organic molecules with valuable applications in various fields.