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3-Chloropropane-1-sulfonyl chloride

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Identification
Molecular formula
C3H6Cl2O2S
CAS number
16283-17-1
IUPAC name
3-chloropropane-1-sulfonyl chloride
State
State
At room temperature, 3-chloropropane-1-sulfonyl chloride is in a liquid state.
Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
95.00
Boiling point (Kelvin)
368.15
General information
Molecular weight
178.05g/mol
Molar mass
178.0540g/mol
Density
1.4595g/cm3
Appearence
3-Chloropropane-1-sulfonyl chloride is a colorless to light-yellow liquid. It has a pungent odor characteristic of chlorinated sulfonyl compounds. Upon exposure to air, it may slowly release hydrochloric acid vapors.
Comment on solubility

Solubility of 3-chloropropane-1-sulfonyl chloride

3-chloropropane-1-sulfonyl chloride, with the chemical formula C3H6ClO2S, exhibits interesting solubility characteristics that can impact its applications:

  • Polarity: This compound is quite polar due to the presence of the sulfonyl chloride group, which is known for enhancing solubility in polar solvents.
  • Solvent Compatibility: It is generally soluble in polar organic solvents, such as:
    • Dichloromethane
    • Acetone
    • Alcohols
  • Water Solubility: While sulfonyl chlorides can exhibit varying degrees of solubility in water, 3-chloropropane-1-sulfonyl chloride has a limited solubility due to its hydrophobic alkyl chain.
  • Influence of Temperature: Increasing temperature usually enhances solubility, allowing for better dissolution in solvents and facilitating reactions.

In summary, the solubility of 3-chloropropane-1-sulfonyl chloride is primarily influenced by its polarity, the nature of the solvent, and temperature conditions. This compound's compatibility with various solvents underlines its versatility in chemical processes.

Interesting facts

Interesting Facts about 3-Chloropropane-1-sulfonyl Chloride

3-Chloropropane-1-sulfonyl chloride is a significant compound in the field of organic chemistry, often utilized in the synthesis of various chemical entities. Here are some fascinating facts about this compound:

  • Reactive Agent: This compound acts as a potent electrophile, making it highly reactive towards nucleophiles. This property is particularly useful in various chemical reactions and synthesis processes.
  • Sulfonyl Chlorides: Compounds featuring sulfonyl chloride functional groups are essential intermediates in organic synthesis. They are frequently employed to produce sulfonamides and other valuable chemical derivatives.
  • Applications: 3-chloropropane-1-sulfonyl chloride serves as a precursor for synthesizing pharmaceuticals, agrochemicals, and dyes. Its versatility allows chemists to create compounds with diverse functionalities.
  • Environmental Considerations: As with many chlorinated organic compounds, the use of 3-chloropropane-1-sulfonyl chloride requires careful handling and consideration of environmental impact, given the potential for toxicity and reactivity.
  • Regulatory Status: Due to its potential uses in industrial applications, understanding the safety regulations concerning this compound is crucial for researchers and manufacturers involved in its handling.

In conclusion, 3-chloropropane-1-sulfonyl chloride is not only valuable as a chemical building block but also serves as an intriguing subject for study in both synthetic and applied chemistry. Its reactivity and diverse applications make it a compound of interest in research and industry alike.

Synonyms
3-Chloropropanesulfonyl chloride
1633-82-5
1-Propanesulfonyl chloride, 3-chloro-
3-Chloro-1-propanesulfonyl chloride
3-Chloropropanesulphonyl chloride
3-Chloropropylsulfonyl chloride
PROPANESULFONYL CHLORIDE, CHLORO-
gamma-Chloropropanesulfonyl chloride
EINECS 216-646-3
26KZB8ERS7
NSC 93777
TL 136
BRN 1754119
NSC-93777
DTXSID30167559
3chloropropanesulfonyl chloride
3Chloropropanesulphonyl chloride
3Chloro1propanesulfonyl chloride
DTXCID9090050
gammaChloropropanesulfonyl chloride
1Propanesulfonyl chloride, 3chloro (8CI)
1-Propanesulfonyl chloride, 3-chloro-(8CI)
1Propanesulfonyl chloride, 3chloro (8CI)(9CI)
1-Propanesulfonyl chloride, 3-chloro-(8CI)(9CI)
216-646-3
3-chloropropane-1-sulfonyl chloride
3-Chloropropanesulfonylchloride
3-CHLORO-PROPANE-1-SULFONYL CHLORIDE
MFCD00007463
3-CHLOROPROPANE SULFONYL CHLORIDE
C3H6Cl2O2S
3-chloropropylsulfonylchloride
1-Chloro-3-propanesulfonyl Chloride; NSC 93777; ?-Chloropropanesulfonyl Chloride;
UNII-26KZB8ERS7
chloropropylsulfonyl chloride
Chloropropanesulfonyl chloride
SCHEMBL68201
3-chloropropanesulfonyl choride
3-chloropropylsulphonyl chloride
3-chloro-propylsulfonyl chloride
3-chloro-propanesulfonyl chloride
3-chloro-propane sulfonyl chloride
3-chloropropane-1-sulfonylchloride
3-Chloro-1-propylsulfonyl chloride
3-chloro-n-propanesulfonyl chloride
ALBB-021306
BCP22287
NSC93777
1-Chloro-3-propanesulfonyl chloride
3-chloro-1-propanesulphonyl chloride
3-Chloropropane-1-sulphonyl chloride
3-chloropropanesulfonic acid chloride
BBL027644
STL370327
.gamma.-Chloropropanesulfonyl chloride
3-chloropropanesulphonic acid chloride
AKOS000121347
3-Chloropropanesulfonyl chloride, 98%
FC07915
FS-4388
3-chloro-1-propanesulfonic acid chloride
DB-006413
NS00025330
EN300-21154
F0001-0587
InChI=1/C3H6Cl2O2S/c4-2-1-3-8(5,6)7/h1-3H