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1-Bromo-3,5-dichlorobenzene

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Identification
Molecular formula
C6H3BrCl2
CAS number
18282-59-2
IUPAC name
1-bromo-3,5-dichloro-benzene
State
State

At room temperature, 1-Bromo-3,5-dichlorobenzene is typically in a liquid state.

Melting point (Celsius)
14.00
Melting point (Kelvin)
287.15
Boiling point (Celsius)
223.00
Boiling point (Kelvin)
496.15
General information
Molecular weight
223.39g/mol
Molar mass
223.3900g/mol
Density
1.7850g/cm3
Appearence

1-Bromo-3,5-dichlorobenzene is a colorless to light yellow liquid. It appears clear and tends to be used in various organic synthesis applications.

Comment on solubility

Solubility of 1-bromo-3,5-dichloro-benzene

1-bromo-3,5-dichloro-benzene, a halogenated aromatic compound, exhibits unique solubility characteristics.

In general, the solubility of halogenated aromatic compounds is influenced by several factors, including:

  • Polarity: The presence of bromine and chlorine atoms increases the polarity of this compound, making it more soluble in polar solvents.
  • Hydrophobicity: However, its aromatic structure and multiple halogen substituents contribute to hydrophobic characteristics, reducing solubility in water.
  • Solvent Interactions: 1-bromo-3,5-dichloro-benzene is more likely to dissolve in organic solvents such as ethyl acetate, toluene, and chloroform.

Generally, 1-bromo-3,5-dichloro-benzene is considered to be insoluble in water, exhibiting a greater affinity for non-polar solvents. This solubility profile is crucial for its applications in organic synthesis and can influence reaction mechanisms.

In summary, while 1-bromo-3,5-dichloro-benzene may be limited in aqueous solubility, it finds utility in a variety of organic environments.

Interesting facts

Interesting Facts about 1-Bromo-3,5-dichloro-benzene

1-Bromo-3,5-dichloro-benzene, a chlorinated aromatic compound, is a significant player in the realm of organic chemistry. Here are some fascinating aspects of this intriguing compound:

  • Environmental Impact: Due to its halogenated nature, this compound can pose environmental risks. Halogenated compounds are often resistant to degradation, leading to potential accumulation in ecosystems.
  • Applications: It serves as an important intermediate in the synthesis of various agrochemicals, pharmaceuticals, and polymers, showcasing its versatility in chemical manufacturing.
  • Reactive Behavior: The presence of both bromine and chlorine atoms on a benzene ring increases the compound's reactivity, making it a valuable candidate for further chemical reactions, such as nucleophilic substitutions.
  • Research Significance: This compound is studied for its properties in the synthesis of more complex molecules, aiding scientists in exploring new pathways for organic synthesis.

As you delve into research and applications of 1-bromo-3,5-dichloro-benzene, remember this key quote: “The beauty of chemistry lies in its capacity to create endless possibilities.” Its structure opens up avenues for innovation in multiple industrial sectors.

In summary, 1-bromo-3,5-dichloro-benzene is more than just a compound; it is a gateway to understanding the deeper connections between chemical structure, reactivity, and environmental considerations.

Synonyms
1-BROMO-3,5-DICHLOROBENZENE
19752-55-7
Benzene, 1-bromo-3,5-dichloro-
EINECS 243-270-7
DTXSID1066524
DTXCID8036150
243-270-7
RefChem:562407
3,5-Dichlorobromobenzene
1-bromo-3,5-dichloro-benzene
MFCD00000584
benzene, 1-bromo-3,5-dichloro
Maybridge1_000881
3,5-Dichloro bromobenzene
3,5-dichloro-1-bromobenzene
AKJ3JR99KS
l-Brom-3,5-dichlorbenzol
3,5-dichloro bromo benzene
SCHEMBL114694
SCHEMBL491558
(3,5-Dichlorophenyl) bromide
SCHEMBL4011077
HMS544A01
STR07058
BTB 03107
CCG-50789
1-Bromo-3,5-dichlorobenzene, 98%
AKOS009156912
AC-7762
CS-W013037
FB151785
SY006090
DB-022034
B2223
NS00026419
ST50405843
EN300-42477
SR-01000640136-1
F0001-0702
Z425865630
InChI=1/C6H3BrCl2/c7-4-1-5(8)3-6(9)2-4/h1-3