6117-80-2
6117-80-2
Chemical Structure
cis-2-Butene-1,4-diol
- CAS No.: 6117-80-2
- Formula:C4H8O2
- Molecular Weight:88.11
IUPAC Name: (Z)-but-2-ene-1,4-diol
InChIKey: ORTVZLZNOYNASJ-UPHRSURJSA-N
SMILES: OC/C=C\CO
Biological Activity: cis-2-Butene-1,4-diol serves as a probe for investigating isomerization and hydrogenation/hydrogenolysis reactions. cis-2-Butene-1,4-diol is also a compound used in the synthesis of the antiviral agent Oxetanocin A. cis-2-Butene-1,4-diol undergoes hydrogenation and hydrogenolysis reactions over supported platinum catalysts, with negligible levels of isomerization[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
cis-2-Butene-1,4-diol | 96.0% | cis-2-Butene-1,4-diol serves as a probe for investigating isomerization and hydrogenation/hydrogenolysis reactions. cis-2-Butene-1,4-diol is also a compound used in the synthesis of the antiviral agent Oxetanocin A. cis-2-Butene-1,4-diol undergoes hydrogenation and hydrogenolysis reactions over supported platinum catalysts, with negligible levels of isomerization. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. M.G. Musolino, et al, cis-2-Butene-1,4-diol as probe for studying isomerization versus hydrogenation and hydrogenolysis reactions, Applied Catalysis A: General, Volume 243, Issue 2, 2003, Pages 333-346, ISSN 0926-860X.
- [2]. Musolino M G, et al. Hydrogenation versus hydrogenolysis in the reaction of cis-2-butene-1, 4-diol over supported platinum catalysts: Kinetic aspects[J]. Applied Catalysis A: General, 2005, 285(1-2): 50-58.
- [3]. Murakami H, et al. Cyclodehydration of cis–2-butene-1, 4-diol with active methylene compounds catalyzed by a diphosphinidenecyclobutene-coordinated palladium complex[J]. Journal of organometallic chemistry, 2006, 691(14): 3151-3156.
- [4]. Liang Y, et al. Access to oxetane-containing psico-nucleosides from 2-methyleneoxetanes: a role for neighboring group participation?. J Org Chem. 2011;76(24):9962-9974. [Content Brief]
