Benzene-1,3-disulfonyl chloride
CAS: 585-47-7
Ref. 3D-FB18181
1g | Discontinued | ||
2g | Discontinued | ||
5g | Discontinued | ||
10g | Discontinued | ||
25g | Discontinued |
Product Information
- 1,3-Benzenedisulfonyl dichloride1,3-Benzenedisulfonyl chloride3-(Chlorosulfonyl)benzenesulfonyl chloride
- 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
- See more synonyms
- m-Benzenedisulfonyl dichloride
- m-Bis(chlorosulfonyl)benzene
- m-Phenylenedisulfonyl chloride
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.