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125199

Sigma-Aldrich

3-Chloropropanesulfonyl chloride

98%

Synonym(s):

γ-Chloropropanesulfonyl chloride, 1-Chloro-3-propanesulfonyl chloride, 3-Chloro-1-propanesulfonyl chloride, 3-Chloro-n-propanesulfonyl chloride, 3-Chloropropylsulfonyl chloride

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$95.90
25 G
$182.50

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5 G
$95.90
25 G
$182.50

About This Item

Linear Formula:
Cl(CH2)3SO2Cl
CAS Number:
1633-82-5
Molecular Weight:
177.05
Beilstein/REAXYS Number:
1754119
EC Number:
216-646-3
MDL number:
MFCD00007463
UNSPSC Code:
12352100
PubChem Substance ID:
24847653
NACRES:
NA.22

$95.90

List Price$137.00Save 30%
Web-Only Promotion

Available to ship onApril 22, 2025Details

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Quality Level

200

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.)

functional group

chloro

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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Application

3-Chloropropanesulfonyl chloride was used as starting reagent in the synthesis of the pyrrolidine-based chiral imidazolium ionic liquid[1]. It was also used in sulfonation of cross-linked polyethylenimine for selective removal of Hg[2]. 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[3] and sultones[4].

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H314,H335

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
0000327665
0000224153
0000279388
0000293606
0000215711

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Functionalized chiral ionic liquid as recyclable organocatalyst for asymmetric Michael addition to nitrostyrenes.
Ni B, et al.
Green Chemistry, 9(7), 737-739 (2007)
Sulfonated cross-linked polyethylenimine for selective removal of mercury from aqueous solutions.
Saad DMG, et al.
Toxicological & Environmental Chemistry, 94(10), 1916-1929 (2012)
Xolisiwe Sebutsoe et al.
Chemosphere, 266, 128975-128975 (2020-11-25)
Arsenic and selenium are both carcinogenic and their presence in fresh water has attracted the development of robust and accurate monitoring techniques. A new diffusive gradients in thin-films (DGT) sampler was developed and evaluated for the in situ measurements of
Catalytic enantio- and diastereoselective formation of beta-sultones: ring-strained precursors for enantioenriched beta-hydroxysulfonyl derivatives.
Florian M Koch et al.
Angewandte Chemie (International ed. in English), 46(15), 2685-2689 (2007-03-03)
Marian Zajac et al.
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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