(1S,4R)-methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate

(1S,4R)-methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate

(1S,2R,3S,5R)-3-(phenylmethoxy)-2-[(phenylmethoxy)methyl]-6-oxabicyclo[3.1.0]hexane

(1S,2R,3S,5R)-3-(phenylmethoxy)-2-[(phenylmethoxy)methyl]-6-oxabicyclo[3.1.0]hexane

(1S,2R)-2-(Benzyloxymethyl)-1-hydroxy-3-cyclopentene

$200.00
CAS No.: 110567-21-0
Catalog No.: 109914
Purity: 95%
MF: C13H16O2
MW: 204.269
Storage: 2-8 degree Celsius
SMILES: O[C@H]1CC=C[C@@H]1COCC1=CC=CC=C1
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(1S,2R)-2-(Benzyloxymethyl)-1-hydroxy-3-cyclopentene; CAS No.: 110567-21-0; This bicyclic cyclopentene diol derivative exemplifies ChemShuttle s building blocks for nucleoside analogs. The (1S,2R)-configuration and benzyloxymethyl group serve as chiral precursors for antiviral prodrug development. Our expertise in asymmetric epoxidation and dihydroxylation ensures high enantiomeric excess. The product s orthogonal protection sites (benzyl ethers) demonstrate our capability to support complex carbohydrate chemistry for nucleotide modifications.

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