Benzene, 1,2-dibromo-4-(bromomethyl)-


Chemical Name: Benzene, 1,2-dibromo-4-(bromomethyl)-
CAS Number: 64382-93-0
Product Number: AG00ETE4(AGN-PC-0NIVAG)
Synonyms:
MDL No:
Molecular Formula: C7H5Br3
Molecular Weight: 328.8266

Identification/Properties


Properties
BP:
323.9±27.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
328.829g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
327.792g/mol
Monoisotopic Mass:
325.794g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
105
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



1,2-Dibromo-4-(bromomethyl)benzene, also known as bromomethyl dibromobenzene, is a versatile compound widely used in chemical synthesis processes. This compound plays a crucial role as a key building block in various organic transformations, particularly in the synthesis of complex organic molecules. One of the significant applications of 1,2-Dibromo-4-(bromomethyl)benzene is in the preparation of pharmaceutical intermediates. Its unique structure and reactivity make it a valuable starting material for the synthesis of various biologically active compounds, such as drugs and agrochemicals. The bromine atoms present in the molecule can undergo diverse chemical reactions, enabling the introduction of functional groups at specific positions in the benzene ring.Moreover, 1,2-Dibromo-4-(bromomethyl)benzene is utilized in the field of material science for the development of advanced polymers and materials with specific properties. By incorporating this compound into polymer chains, researchers can tailor the material's characteristics, such as thermal stability, mechanical strength, and chemical resistance.Additionally, this compound finds application in the production of specialty chemicals, dyes, and fine chemicals. Its ability to undergo substitution reactions allows for the generation of a wide range of derivatives with varying properties, enabling the synthesis of bespoke chemical compounds for specific industrial purposes.Overall, 1,2-Dibromo-4-(bromomethyl)benzene serves as a crucial building block in organic synthesis, offering chemists a valuable tool for designing and developing complex molecules with targeted functionalities and applications.