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3-Bromobenzenesulfonyl chloride

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Identification
Molecular formula
C6H4BrClO2S
CAS number
17472-02-1
IUPAC name
3-bromobenzenesulfonyl chloride
State
State

At room temperature, 3-Bromobenzenesulfonyl chloride is typically in a solid state.

Melting point (Celsius)
64.00
Melting point (Kelvin)
337.15
Boiling point (Celsius)
299.80
Boiling point (Kelvin)
572.95
General information
Molecular weight
255.52g/mol
Molar mass
255.5180g/mol
Density
1.6788g/cm3
Appearence

3-Bromobenzenesulfonyl chloride appears as a white to light yellow crystalline solid. Its appearance may vary slightly depending on the purity and specific conditions.

Comment on solubility

Solubility of 3-bromobenzenesulfonyl chloride

3-bromobenzenesulfonyl chloride, with its unique structure, exhibits particular solubility characteristics that are essential for its practical applications in organic synthesis. This compound, being a sulfonyl chloride, demonstrates a range of solubility behaviors in different solvents:

  • Soluble in Organic Solvents: 3-bromobenzenesulfonyl chloride is typically soluble in organic solvents such as dichloromethane, diethyl ether, and acetone. This property makes it suitable for use in organic reaction environments.
  • Low Solubility in Water: The presence of the sulfonyl chloride functional group suggests that it has limited solubility in water. This is primarily due to the hydrophobic aromatic ring which counterbalances the polar nature of the sulfonyl chloride.
  • Temperature Dependence: Like many chemical compounds, the solubility of 3-bromobenzenesulfonyl chloride may vary with temperature. Generally, increasing the temperature can enhance solubility in organic solvents.
  • Conductivity: In solution, the dissociation of the sulfonyl chloride group allows for increased ionic activity, though this is more relevant in organic matrices than in aqueous systems.

In conclusion, understanding the solubility of 3-bromobenzenesulfonyl chloride is crucial for effective application in chemical reactions. Its solubility properties not only dictate its usability but also underscore the importance of solvent choice in chemical processes.

Interesting facts

Interesting Facts about 3-Bromobenzenesulfonyl Chloride

3-Bromobenzenesulfonyl chloride is a fascinating chemical compound that plays a significant role in organic synthesis and medicinal chemistry. Here are some intriguing aspects of this compound:

  • Reactivity: This compound is renowned for its electrophilic substitution reactions, making it a valuable intermediate for creating various sulfonated compounds.
  • Functional Groups: The presence of both a –Br (bromo) and a –SO2Cl (sulfonyl chloride) group allows for diverse reactivity. Each functional group contributes unique properties to the compound.
  • Synthesis Applications: It is commonly used in the synthesis of pharmaceuticals and agrochemicals, helping to produce compounds with anti-inflammatory and antibacterial properties.
  • Environmental Considerations: Researchers are continually exploring methods to utilize this compound in cleaner and more sustainable processes, showcasing the importance of environmental responsibility in chemistry.
  • Historical Significance: Understanding the chemistry of sulfonyl chlorides has paved the way for advancements in synthetic pathways, bringing us closer to innovative drug discovery and development.

As noted by chemist David G. Leith, "The versatility of sulfonyl chlorides like 3-bromobenzenesulfonyl chloride ensures their relevance in contemporary organic chemistry." This compound serves as a reminder of the intricate relationship between structure and function in the realm of chemical science.


In conclusion, 3-bromobenzenesulfonyl chloride is not just a simple chemical; it is a crucial building block in the world of chemistry, exhibiting extensive applications and reactivity that fuel ongoing research and development.

Synonyms
2905-24-0
3-bromobenzene-1-sulfonyl chloride
M-BROMOBENZENESULPHONYL CHLORIDE
DTXSID60183287
DTXCID70105778
628-300-2
3-Bromobenzenesulfonyl chloride
3-Bromobenzenesulphonyl Chloride
Benzenesulfonyl chloride, 3-bromo-
m-bromobenzenesulfonyl chloride
3-bromo-benzenesulfonyl chloride
MFCD00052313
3-bromobenzenesulfonylchloride
3-bromobenzene sulfonyl chloride
3-bromophenylsulfonyl chloride
3-bromobenzensulfonyl chloride
SCHEMBL101963
3-bromobenzenesulfonyl-chloride
3-bromophenylsulphonyl chloride
3-bromophenyl sulfonyl chloride
3-bromo benzenesulfonyl chloride
3-bromophenyl sulphonyl chloride
3-bromobenzene sulphonyl chloride
3-bromanylbenzenesulfonyl chloride
3-bromo-benzene sulfonyl chloride
3-Bromobenzenesulfonyl chloride, 96%
AKOS001063765
AB02184
CS-W007356
FB46315
AS-18789
DB-013114
B2389
EN300-06828
A819737
Z56933874
3-Bromobenzene-1-sulfonyl Chloride; 3-Bromophenylsulfonyl Chloride; m-Bromobenzenesulfonyl Chloride