All Photos(2)
γ-Chloropropanesulfonyl chloride, 1-Chloro-3-propanesulfonyl chloride, 3-Chloro-1-propanesulfonyl chloride, 3-Chloro-n-propanesulfonyl chloride, 3-Chloropropylsulfonyl chloride
Cl(CH2)3SO2Cl
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Quality Level
Assay
98%
form
liquid
refractive index
n20/D 1.489 (lit.)
bp
70 °C/0.5 mmHg (lit.)
density
1.456 g/mL at 25 °C (lit.)
SMILES string
ClCCCS(Cl)(=O)=O
InChI
1S/C3H6Cl2O2S/c4-2-1-3-8(5,6)7/h1-3H2
InChI key
GPKDGVXBXQTHRY-UHFFFAOYSA-N
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Related Categories
Application
3-Chloropropanesulfonyl chloride was used as starting reagent in the synthesis of the pyrrolidine-based chiral imidazolium ionic liquid. It was also used in sulfonation of cross-linked polyethylenimine for selective removal of Hg. It was used in generation and trapping of the derived sulfene with imines and glyoxylates in the presence of chinchona alkaloids to yield chiral sultams and sultones.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Catalytic enantio- and diastereoselective formation of beta-sultones: ring-strained precursors for enantioenriched beta-hydroxysulfonyl derivatives.
Angewandte Chemie (International ed. in English), 46(15), 2685-2689 (2007-03-03)
Sulfonated cross-linked polyethylenimine for selective removal of mercury from aqueous solutions.
Toxicological & Environmental Chemistry, 94(10), 1916-1929 (2012)
Functionalized chiral ionic liquid as recyclable organocatalyst for asymmetric Michael addition to nitrostyrenes.
Green Chemistry, 9(7), 737-739 (2007)
Organic letters, 9(10), 2007-2010 (2007-04-24)
beta-Sultams, highly strained sulfonyl analogues of beta-lactams, were prepared enantio- and diastereoselectively by tertiary amine catalyzed [2 + 2] cycloaddition reactions. The title compounds are practical precursors of highly enantioenriched biologically interesting beta-aminosulfonyl derivatives.
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