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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)-

Methane, bromoiodo-

BrCI Request for Quotation
Chemical Name: Methane, bromoiodo-
CAS Number: 557-68-6
Product Number: AG003OKL(AGN-PC-0JL8G0)
Synonyms:
MDL No:
Molecular Formula: CH2BrI
Molecular Weight: 220.8350

Identification/Properties

Properties
BP:
139.5°C
Storage:
Light sensitive;Keep in dry area;2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.6382(lit.)
Computed Properties
Molecular Weight:
220.835g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
219.838g/mol
Monoisotopic Mass:
219.838g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
3
Formal Charge:
0
Complexity:
4.8
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:
H315-H318-H335
Precautionary Statements:
P280-P302+P352-P305+P351+P338+P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Bromoiodomethane, also known as methyl bromoiodide, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, Bromoiodomethane is commonly employed as a halogenating agent, particularly in the introduction of the bromoiodo functional group into various molecules. This compound serves as a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, Bromoiodomethane is utilized in the preparation of intermediates for complex organic reactions, such as the Heck and Suzuki coupling reactions, where its dual halogen nature plays a crucial role in the formation of new carbon-carbon bonds. This compound's ability to efficiently substitute hydrogen atoms with bromine and iodine atoms makes it an essential tool in the manipulation of molecular structures and the creation of novel compounds in the field of organic synthesis.