1135339-49-9 | rac-2,3-Dehydro-3,4-dihydro Ivermectin

Packsize	Purity	Availability	Price	Discounted Price
1mg		2 weeks	$1,374.00	$962.00

Description

• Catalog Number: AE15742
• Chemical Name: rac-2,3-Dehydro-3,4-dihydro Ivermectin
• CAS Number: 1135339-49-9
• Molecular Formula: C48H74O14
• Molecular Weight: 875.0928
• SMILES: CO[C@H]1C[C@H](O[C@H]2[C@@H](C)/C=C/C=C/3CO[C@H]4[C@]3(O)C(=CC([C@H]4O)C)C(=O)O[C@H]3C[C@@H](C/C=C/2C)O[C@]2(C3)CC[C@@H]([C@H](O2)[C@H](CC)C)C)O[C@H]([C@@H]1O[C@H]1C[C@H](OC)[C@H]([C@@H](O1)C)O)C

Upstream Synthesis Route

(4S)-2,3-Didehydro-5-O-demethyl-3,4,22,23-tetrahydroavermectin A1a, a derivative of the widely-used avermectin class of compounds, serves as a valuable tool in chemical synthesis. This compound's unique structural elements make it an ideal reagent for various synthetic transformations and reactions.In chemical synthesis, (4S)-2,3-Didehydro-5-O-demethyl-3,4,22,23-tetrahydroavermectin A1a can act as a versatile building block for creating complex molecules with specific functionalities. Its presence can enable the introduction of specific chemical groups or modifications at various positions within a target molecule, facilitating the generation of novel compounds with tailored properties.Additionally, the chirality of (4S)-2,3-Didehydro-5-O-demethyl-3,4,22,23-tetrahydroavermectin A1a enhances its utility in asymmetric synthesis, where the stereochemical outcome of a reaction is crucial. By utilizing this compound as a chiral auxiliary or as a starting material, chemists can access enantiomerically pure products, essential in the pharmaceutical, agrochemical, and materials science industries.Overall, the strategic incorporation of (4S)-2,3-Didehydro-5-O-demethyl-3,4,22,23-tetrahydroavermectin A1a in chemical synthesis offers a powerful approach to designing and accessing structurally diverse molecules with tailored properties and applications.