65291-30-7
65291-30-7
Chemical Structure
(R)-(+)-Trityl glycidyl ether
- CAS No.: 65291-30-7
- Formula:C22H20O2
- Molecular Weight:316.39
IUPAC Name: (R)-2-((trityloxy)methyl)oxirane
InChIKey: XFSXUCMYFWZRAF-OAQYLSRUSA-N
SMILES: [C@@H]1(CO1)COC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
Biological Activity: (R)-(+)-Trityl glycidyl ether, a heterocyclic compound, is a precursor that can be used to synthesize glycerophospholipids, as well as compounds with antiviral and antimalarial activities[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(R)-(+)-Trityl glycidyl ether | 97.0% | (R)-(+)-Trityl glycidyl ether, a heterocyclic compound, is a precursor that can be used to synthesize glycerophospholipids, as well as compounds with antiviral and antimalarial activities. | ||||||||||||||||||||
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References
- [1]. Baszczyňski O, et al. Synthesis and antiviral activity of N9-[3-fluoro-2-(phosphonomethoxy)propyl] analogues derived from N6-substituted adenines and 2,6-diaminopurines. Bioorg Med Chem. 2011 Apr 1;19(7):2114-24. [Content Brief]
- [2]. Sato E, et al. Design, synthesis and anti-malarial activities of synthetic analogs of biselyngbyolide B, a Ca2+ pump inhibitor from marine cyanobacteria. Bioorg Med Chem Lett. 2018 Feb 1;28(3):298-301. [Content Brief]
Keywords
