Benzene, 1-bromo-3-(bromomethyl)-2-methyl-


Chemical Name: Benzene, 1-bromo-3-(bromomethyl)-2-methyl-
CAS Number: 112299-62-4
Product Number: AG003E3P(AGN-PC-03UMEL)
Synonyms:
MDL No:
Molecular Formula: C8H8Br2
Molecular Weight: 263.9571

Identification/Properties


Properties
MP:
31-32 °C
BP:
278.749°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
263.96g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
263.897g/mol
Monoisotopic Mass:
261.899g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
103
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-3-(bromomethyl)-2-methylbenzene, also known as (1-bromo-3-bromo-2-methylphenyl)methane, is a versatile compound commonly employed in chemical synthesis. This compound plays a crucial role in the formation of various organic compounds due to its unique chemical reactivity.As a key reagent in organic chemistry, 1-Bromo-3-(bromomethyl)-2-methylbenzene is frequently utilized in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and specialty chemicals. Its bromine substituent provides sites for further chemical modifications, enabling the introduction of various functional groups into the molecular structure.In particular, this compound is valued for its ability to serve as a halogenated building block in the preparation of biologically active compounds. By serving as a starting material or intermediate in organic transformations, 1-Bromo-3-(bromomethyl)-2-methylbenzene enables chemists to access a wide range of structurally diverse products with tailored properties.Moreover, the presence of multiple halogen atoms in the molecule imparts unique reactivity patterns, allowing for selective transformations and facilitating the synthesis of intricate molecular frameworks. Through strategic utilization in multi-step synthetic sequences, 1-Bromo-3-(bromomethyl)-2-methylbenzene contributes to the efficient construction of target molecules with high levels of structural complexity and functional diversity.