1,4-Diazoniabicyclo[2.2.2]octane-1,4-disulfinate
![1,4-Diazoniabicyclo[2.2.2]octane-1,4-disulfinate Structure](https://www.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 | |
Use of 1,4-Diazoniabicyclo[2.2.2]octane-1,4-disulfinateDABCO-Bis(sulfur dioxide) (DABSO) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| Name | 1,4-Diazoniabicyclo[2.2.2]octane-1,4-disulfinate |
|---|---|
| Synonym | More Synonyms |
| Description | DABCO-Bis(sulfur dioxide) (DABSO) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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| Related Catalog |
| Molecular Formula | C6H12N2O4S2 |
|---|---|
| Molecular Weight | 240.30 |
| Exact Mass | 240.02400 |
| PSA | 157.18000 |
| LogP | 0.31460 |
| Storage condition | 2-8°C |
| Symbol |
GHS02, GHS07 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H228-H302-H315-H319-H335-H412 |
| Precautionary Statements | P210-P261-P273-P305 + P351 + P338 |
| RIDADR | UN1325 - class 4.1 - PG 2 - Flammable solids, organic, n.o.s., HI: all |
| HS Code | 2933990090 |
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~99%
1,4-Diazoniabic... CAS#:119752-83-9 |
| Literature: Woolven, Holly; Gonzalez-Rodriguez, Carlos; Marco, Isabel; Thompson, Amber L.; Willis, Michael C. Organic Letters, 2011 , vol. 13, # 18 p. 4876 - 4878 |
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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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-Dialkylhydrazine... |
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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 sulf... |
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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 ... |
| diazabicyclooctane |
| TEDA-L33 |
| dabcos-25 |
| dabco33lv |
| BACO |
| DABCO |
| 1,4-Diazabicyclo[2.2.2]octane bis(sulfur dioxide) adduct |
| TED |
| teda |
| dabcoeg |