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About This Item
Linear Formula:
Cl(CH2)3SO2Cl
CAS Number:
Molecular Weight:
177.05
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-646-3
Beilstein/REAXYS Number:
1754119
MDL number:
Assay:
98%
Form:
liquid
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.)
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
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.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
wgk
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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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)
Sulfonated cross-linked polyethylenimine for selective removal of mercury from aqueous solutions.
Saad DMG, et al.
Toxicological & Environmental Chemistry, 94(10), 1916-1929 (2012)
Functionalized chiral ionic liquid as recyclable organocatalyst for asymmetric Michael addition to nitrostyrenes.
Ni B, et al.
Green Chemistry, 9(7), 737-739 (2007)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 125199-5G | 04061837254048 |
| 125199-25G | 04061837254031 |

