1,4-Diazoniabicyclo[2.2.2]octane-1,4-disulfinate
![1,4-Diazoniabicyclo[2.2.2]octane-1,4-disulfinate Structure](https://image.chemsrc.com/caspic/393/119752-83-9.png)
1,4-Diazoniabicyclo[2.2.2]octane-1,4-disulfinate structure
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Common Name | 1,4-Diazoniabicyclo[2.2.2]octane-1,4-disulfinate | ||
|---|---|---|---|---|
| CAS Number | 119752-83-9 | Molecular Weight | 240.30 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C6H12N2O4S2 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS02, GHS07 |
Signal Word | Danger | |
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Palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides: scope of the three-component synthesis of N-aminosulfonamides.
Org. Biomol. Chem. 10 , 4007-4014, (2012) By using DABCO·(SO(2))(2), DABSO, as a solid bench-stable SO(2)-equivalent, the palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides has been achieved. N,N-Dialkylhydrazines are employed as the N-nucleophiles and provide N-aminosul... |
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DABCO-bis(sulfur dioxide), DABSO, as a convenient source of sulfur dioxide for organic synthesis: utility in sulfonamide and sulfamide preparation.
Org. Lett. 13 , 4876-4878, (2011) The charge-transfer complex generated from the combination of DABCO and sulfur dioxide, DABSO, is a bench-stable colorless solid suitable for use in organic synthesis as a replacement for gaseous sulfur dioxide. The complex can be combined with Grignard reage... |
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Palladium-catalyzed aminosulfonylation of aryl halides.
J. Am. Chem. Soc. 132 , 16372-16373, (2010) The palladium-catalyzed three-component coupling of aryl iodides, sulfur dioxide, and hydrazines to deliver aryl N-aminosulfonamides is described. The colorless crystalline solid DABCO·(SO(2))(2) was used as a convenient source of sulfur dioxide. The reaction... |