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About This Item
Linear Formula:
Cl2C6H3SO2Cl
CAS Number:
Molecular Weight:
245.51
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
95%
refractive index
n20/D 1.589 (lit.)
bp
253 °C (lit.)
density
1.572 g/mL at 25 °C (lit.)
SMILES string
Clc1ccc(cc1Cl)S(Cl)(=O)=O
InChI
1S/C6H3Cl3O2S/c7-5-2-1-4(3-6(5)8)12(9,10)11/h1-3H
InChI key
NYIBPWGZGSXURD-UHFFFAOYSA-N
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
134.6 °F - closed cup
Flash Point(C)
57 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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D W Combs et al.
Journal of medicinal chemistry, 38(25), 4880-4884 (1995-12-08)
A novel series of nonsteroidal heterocycles was discovered which display cell-type selective, high-affinity (nanomolar) binding to the progesterone receptors from TE85 osteosarcoma cells but > 1 microM binding affinity to the progesterone receptors from T47D and ZR75 human breast carcinoma
Whitney Beysselance Moro et al.
Journal of combinatorial chemistry, 11(4), 617-625 (2009-05-05)
A new lead class of antibacterial drug-like NAD synthetase (NADs) inhibitors was previously identified from a virtual screening study. Here a solution-phase synthetic library of 76 compounds, analogs of the urea-sulfonamide 5838, was synthesized in parallel to explore SAR on
4-Allyl-2-methoxyphenyl 3, 4-dichlorobenzenesulfonate.
Ma Y-T, et al.
Acta Crystallographica Section E, Structure Reports Online, 67(11), 3082-3082 (2011)
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