cas 80358-06-1|| where to buy Tinnevellin glucoside

Nombre del producto:Tinnevellin glucoside

IUPAC Name:1-(1-hydroxy-8-methoxy-3-methyl-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}naphthalen-2-yl)ethan-1-one

Unidad de embalaje	Stock disponible	Precio($)
CM578708-10mg	in stock	ƴŞǫ
CM578708-25mg	in stock	ŪŪƐ

Sólo para uso en I+D..

Formulario de consulta

Nombre químico

Número CAS

Cantidad*

Especificaciones requeridas*
(% de ensayo, grado de material, etc.)

Nombre de contacto*

Correo electrónico de contacto*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 80358-06-1 regularly via the above email.

Notas adicionales

Verification code*

refresh

: Núm. De CAS :80358-06-1; Fórmula molecular:C20H24O9; Punto de fusión:-; Código de sonrisas:CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O; Densidad:

: Número de catálogo:CM578708; Peso molecular:408.4; Punto de ebullición:; Nº Mdl:MFCD28964208; Almacenamiento:

: Naphthalenes; Naphthalene is a hydrocarbon produced by the distillation of coal tar and is an aromatic white crystalline substance. Naphthalene is the most abundant component in coal tar. It is used as an insect repellant and insect fumigant. The compound is used in the manufacture of celluloid, dyes, hydrogenated naphthalenes, oil fumes, smokeless powders and synthetic resins.

: 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.