CAS 1633-82-5

3-Chloropropanesulfonyl chloride

Description:

3-Chloropropanesulfonyl chloride, with the CAS number 1633-82-5, is an organosulfur compound characterized by the presence of both a sulfonyl chloride and a chloroalkyl group. It typically appears as a colorless to pale yellow liquid and is known for its reactivity, particularly due to the sulfonyl chloride functional group, which can readily participate in nucleophilic substitution reactions. This compound is soluble in organic solvents such as dichloromethane and ether but is generally insoluble in water. It is used in organic synthesis as a reagent for introducing sulfonyl groups into various substrates, making it valuable in the production of pharmaceuticals and agrochemicals. However, it is also important to handle this compound with care, as it can be corrosive and may cause irritation to the skin, eyes, and respiratory system. Proper safety precautions, including the use of personal protective equipment, are essential when working with this substance in a laboratory setting.

Formula: C₃H₆Cl₂O₂S

InChI: InChI=1S/C3H6Cl2O2S/c4-2-1-3-8(5,6)7/h1-3H2

InChI key: InChIKey=GPKDGVXBXQTHRY-UHFFFAOYSA-N

SMILES: C(S(Cl)(=O)=O)CCCl

Synonyms:

• 1-Chloro-3-propanesulfonyl chloride
• 1-Propanesulfonyl chloride, 3-chloro-
• 3-Chloro-1-propanesulfonyl chloride
• 3-Chloro-n-propanesulfonyl chloride
• 3-Chloropropane-1-sulfonyl chloride
• 3-Chloropropanesulfonyl
• 3-Chloropropanesulfonylchloride
• 3-Chloropropanesulphonyl chloride
• 3-Chloropropansulfonyl chloride
• 3-Chloropropylsulfonyl chloride
• NSC 93777
• γ-Chloropropanesulfonyl chloride

3-Chloropropanesulfonyl Chloride

CAS: 1633-82-5

Formula: C₃H₆Cl₂O₂S

Purity: >95.0%(GC)(T)

Molecular weight: 177.04

Ref: 3B-C1895

3-Chloropropanesulfonyl chloride, 98+%

CAS: 1633-82-5

3-Chloropropanesulfonyl Chloride is an intermediate used in the preparation of many enzymatic inhibitors. It is also used in the generation and trapping of the derived sulfene with imines and glyoxylates in the presence of chinchona alkaloids provide chiral sultams and sultones. It is mainly used f

Formula: C₃H₆Cl₂O₂S

Purity: 98+%

Color and Shape: Clear colorless to yellow to orange or pale brown, Liquid

Molecular weight: 177.04

Ref: 02-A10631

3-Chloropropane-1-sulphonyl chloride

CAS: 1633-82-5

3-Chloropropane-1-sulphonyl chloride

Formula: C₃H₆Cl₂O₂S

Purity: 95%

Color and Shape: colourless - yellow Liquid

Molecular weight: 177.04953

Ref: 54-OR5825

3-chloropropane-1-sulfonyl chloride

CAS: 1633-82-5

Formula: C₃H₆Cl₂O₂S

Purity: 98%

Color and Shape: Liquid

Molecular weight: 177.0495

Ref: IN-DA001U0B

3-Chloropropane-1-sulfonyl chloride

CAS: 1633-82-5

3-Chloropropane-1-sulfonyl chloride

Formula: C₃H₆Cl₂O₂S

Purity: 98%

Molecular weight: 177.05

Ref: IN-DG32180

3-Chloro-propane-1-sulfonyl chloride

CAS: 1633-82-5

Formula: C₃H₆Cl₂O₂S

Purity: 97%

Color and Shape: Liquid

Molecular weight: 177.04

Ref: 10-F049263

3-Chloro-1-propanesulfonyl chloride

CAS: 1633-82-5

3-Chloro-1-propanesulfonyl chloride is a synthetic, bifunctional compound that has been shown to have the ability to inhibit cholesterol acyltransferase and cell culture. 3-Chloro-1-propanesulfonyl chloride has also been shown to bind to the 5-ht4 receptor in vivo and in vitro. It is hydrolyzed by trifluoroacetic acid, which can lead to uptake of the compound into cells. The hydroxy group on 3-chloro-1-propanesulfonyl chloride allows for hydrogen bonding with other molecules, such as fatty acids and matrix metalloproteinases. This property may be responsible for its uptake into cellular structures. 3-Chloro-1-propanesulfonyl chloride has been found in wastewater samples at concentrations between 0.07 - 1 micrograms per liter. In cell cultures, it has been shown to inhibit matrix met

Formula: C₃H₆Cl₂O₂S

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 177.05 g/mol

Ref: 3D-FC07915