4,4-Dimethyl-3,5,8-trioxabic-yclo[5,1,0]Octane
4,4-Dimethyl-3,5,8-trioxabic-yclo[5,1,0]Octane Basic information
- Product Name:
- 4,4-Dimethyl-3,5,8-trioxabic-yclo[5,1,0]Octane
- Synonyms:
-
- 4,4-Dimethyl-3,5,8-trioxabic-yclo[5,1,0]Octane
- 3,5,8-Trioxabicyclo[5.1.0]octane, 4,4-diMethyl-
- 4,4-diMethyl-3,5,8-trioxabicyclo[5.1.0]octane(EP2)
- 4,4-Dimethyl-3,5,8-trioxabic-yclo[5.1.0]octane(DTC-octane)
- Gadobutrol Impurity 49
- 4 4-DIMETHYL-3 5 8-TRIOXABICYCLO (5.1.0)OCTANE TOBO
- 0]Octane
- 4-Dimethyl-3
- CAS:
- 57280-22-5
- MF:
- C7H12O3
- MW:
- 144.17
- EINECS:
- 421-750-9
- Product Categories:
-
- 57280-22-5
- Mol File:
- 57280-22-5.mol
4,4-Dimethyl-3,5,8-trioxabic-yclo[5,1,0]Octane Chemical Properties
- Boiling point:
- 179℃
- Density
- 1.071
- refractive index
- 1.4560 to 1.4600
- Flash point:
- 56℃
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- clear liquid
- color
- Colorless to Light yellow to Light orange
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36-43
- Safety Statements
- 26-36/37-24/25
- HS Code
- 29329990
4,4-Dimethyl-3,5,8-trioxabic-yclo[5,1,0]Octane Usage And Synthesis
Chemical Properties
Clear colorless to yellow liquid
Uses
4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane is used in the CO2-mediated formation of chiral carbamates from meso-epoxides via polycarbonate intermediates and amine nucleophiles, which opens up a wide a wide range of CO2-based carbamate scaffolds with excellent yields and 99% enantiomeric excess.
Application
4, 4-dimethyl-3,5, 8-trioxane [5,1,0] octane is a key intermediate in the preparation of gadobinol. As a meso epoxide, it could be used to obtain optically pure ABT derivatives through Ti(IV)/BINOL catalyzed asymmetric aminolysis[1].
References
[1] Bao H, et al. Insight into the Mechanism of the Asymmetric Ring-Opening Aminolysis of 4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane Catalyzed by Titanium/BINOLate/Water System: Evidence for the Ti(BINOLate)2-Bearing Active Catalyst Entities and the Role of Water. Journal of the American Chemical Society, 2008; 130: 10116–10127.
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