cas 2609644-29-1|| where to buy methyl (1R,3R,4R,5S)-3-[(2R,3R,4R,5R,6R)-3-(allyloxycarbonylamino)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-5-ethyl-4-[(2S,3S,4R,5R,6S)-3,4,5-tribenzyloxy-6-methyl-tetrahydropyran-2-yl]oxy-cyclohexanecarboxylate

Nom du produit:methyl (1R,3R,4R,5S)-3-[(2R,3R,4R,5R,6R)-3-(allyloxycarbonylamino)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-5-ethyl-4-[(2S,3S,4R,5R,6S)-3,4,5-tribenzyloxy-6-methyl-tetrahydropyran-2-yl]oxy-cyclohexanecarboxylate

IUPAC Name:methyl (1R,3R,4R,5S)-3-{[(2R,3R,4R,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(prop-2-en-1-yloxy)carbonyl]amino}oxan-2-yl]oxy}-5-ethyl-4-{[(2S,3S,4R,5R,6S)-3,4,5-tris(benzyloxy)-6-methyloxan-2-yl]oxy}cyclohexane-1-carboxylate

: CAS：2609644-29-1; Formule moléculaire：C47H61NO14; Pureté：95%+

: Numéro de catalogue：CM1018830; Poids moléculaire：864

Unité d'emballage	Stock disponible	Prix($)
CM1018830-100mg	in stock	Ƅƞ
CM1018830-250mg	in stock	ŉǵư
CM1018830-10g	in stock	ŉƞƄĽ
CM1018830-25g	in stock	ȎȎȎǵ

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: N° CAS:2609644-29-1; Formule moléculaire:C47H61NO14; Point de fusion:-; Code SMILES:CC[C@H]1C[C@H](C[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2NC(=O)OCC=C)[C@@H]1O[C@@H]1O[C@@H](C)[C@@H](OCC2=CC=CC=C2)[C@@H](OCC2=CC=CC=C2)[C@@H]1OCC1=CC=CC=C1)C(=O)OC; Densité:

: Numéro de catalogue:CM1018830; Poids moléculaire:864; Point d'ébullition:; N° Mdl:; Stockage:

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: Cyclohexanes; Cyclohexane is an organic compound with a chemical formula C6H12. It is a colorless liquid with a pungent odor, insoluble in water, and soluble in most organic solvents such as ethanol, ether, benzene, and acetone. Cyclohexyl fragments are a common structure in both natural and synthetic drugs. It can be used as both core structure and part of achiral side chain.

: Tetrahydropyrans; Tetrahydropyran is an organic compound consisting of a saturated six-membered ring containing five carbon atoms and one oxygen atom. Tetrahydropyrans are common structural motifs in natural products and synthetic therapeutic molecules. In nature, these six-membered oxygen heterocycles are usually assembled by intramolecular reactions, including oxygen Michael addition or ring opening of epoxy alcohols. In fact, polyether natural products have been particularly extensively studied for their fascinating structures and important biological properties; these are often formed through endoselective epoxy open cascades.

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