CAS 585-47-7: 1,3-Benzenedisulfonyl dichloride
Formula:C6H4Cl2O4S2
InChI:InChI=1S/C6H4Cl2O4S2/c7-13(9,10)5-2-1-3-6(4-5)14(8,11)12/h1-4H
InChI key:InChIKey=ALIQZUMMPOYCIS-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=CC(S(Cl)(=O)=O)=CC=C1
Synonyms:- 1,3-Benzenedisulfonyl chloride
- 1,3-Benzenedisulfonyl dichloride
- 1,3-Bis(chlorosulfonyl)benzene
- 1,3-Phenylenebis(sulfonyl chloride)
- 3-(Chlorosulfonyl)benzenesulfonyl chloride
- 3-Chlorosulfonylbenzenesulfonyl chloride
- Benzene-1,3-Disulfonyl Dichloride
- Nsc 61429
- m-Benzenedisulfonyl chloride
- m-Benzenedisulfonyl dichloride
- m-Bis(chlorosulfonyl)benzene
- See more synonyms
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Found 7 products.
benzene-1,3-disulphonyl dichloride
CAS:benzene-1,3-disulphonyl dichlorideFormula:C6H4Cl2O4S2Purity:98%Color and Shape: white powderMolecular weight:275.13g/molBenzene-1,3-disulfonyl dichloride
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:275.1099853515625Benzene-1,3-disulfonyl dichloride
CAS:Formula:C6H4Cl2O4S2Purity:97%Color and Shape:SolidMolecular weight:275.12956000000011,3-Benzenedisulfonyl dichloride
CAS:1,3-Benzenedisulfonyl dichloride is a bioactive chemical.Formula:C6H4Cl2O4S2Color and Shape:Light Brown SolidMolecular weight:275.131,3-Benzenedisulfonyl Chloride
CAS:Formula:C6H4Cl2O4S2Purity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:275.111,3-Benzenedisulfonyl chloride, 97%
CAS:1,3-Benzenedisulfonyl chloride is used as a pharmaceutical intermediates. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C6H4Cl2O4S2Purity:97%Color and Shape:White to cream to pale brown, Crystals or crystalline powderMolecular weight:275.11Benzene-1,3-disulfonyl chloride
CAS:Benzene-1,3-disulfonyl chloride (BDSC) is an ester that can be used as a model system for hydrogen bond interactions. BDSC has high values and is acidic, which makes it an ideal candidate for use in cervical cancer research. BDSC also has a desymmetrization reaction that occurs when the molecule is exposed to an acidic environment. This process generates the sulfenamide and sulfone functional groups on BDSC. The synthesis of BDSC can be achieved through a number of different methods, including asymmetric synthesis or nucleophilic attack by chloride ions. These reactions are facilitated by crosslinkers such as diazomethane or dimethylsulfate.Formula:C6H4Cl2O4S2Purity:Min. 95%Molecular weight:275.13 g/molRef: 3D-FB18181
Discontinued product
