InChI key
YBBRCQOCSYXUOC-UHFFFAOYSA-N
InChI
1S/Cl2O2S/c1-5(2,3)4
SMILES string
ClS(Cl)(=O)=O
grade
SAJ first grade
vapor density
4.7 (vs air)
vapor pressure
100 mmHg ( 17.8 °C), 105 mmHg ( 20 °C)
assay
≥90.0%
form
liquid
availability
available only in Japan
bp
68-70 °C (lit.)
mp
−54 °C (lit.)
density
1.665 g/mL at 20 °C (lit.)
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Eye Dam. 1 - Skin Corr. 1C - STOT SE 3
target_organs
Respiratory system
supp_hazards
存储类别
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 1
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Christopher Blackburn
ACS combinatorial science, 14(3), 150-154 (2012-02-11)
Reductive aminations and further transformations of an azo dye and fluorous tagged aldehyde are described. The intensely colored 2,4-dialkoxybenzyl protected amines undergo Fmoc-based peptide coupling, Suzuki reactions, and sulfonamide formation with product isolation facilitated by visual monitoring of fluorous solid
Zhiyong Wu et al.
Organic letters, 15(6), 1270-1273 (2013-03-07)
An efficient and concise one-pot protocol to synthesize sulfonylated quinoline N-oxides via copper-catalyzed C-H bond activation has been developed. Commercially available and less expensive aryl sulfonyl chlorides were used as the sulfonylation reagents. Various 2-aryl sulfonyl quinolines were obtained in
Polystyrene sulfonyl chloride: a highly orthogonal linker resin for the synthesis of nitrogen-containing heterocycles.
Matthias Mentel et al.
Angewandte Chemie (International ed. in English), 48(32), 5841-5844 (2009-07-08)
Iron-catalyzed desulfinylative C-C cross-coupling reactions of sulfonyl chlorides with grignard reagents.
Chandra M Rao Volla et al.
Angewandte Chemie (International ed. in English), 47(7), 1305-1307 (2008-01-05)
Michael Harmata et al.
The Journal of organic chemistry, 72(2), 683-685 (2007-01-16)
Sulfinamides were synthesized from sulfonyl chlorides using a procedure involving in situ reduction of sulfonyl chlorides. The reaction is broad in scope and easy to perform.
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