The chemical substance known as (3aS,6S)-6-methoxy-2,2,4-trimethyl-4,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-ol, with the CAS number 71772-35-5, is a complex organic compound characterized by its unique bicyclic structure that incorporates a dioxole and pyran moiety. This compound features multiple methyl groups, contributing to its hydrophobic nature and potentially influencing its solubility and reactivity. The presence of a methoxy group enhances its chemical properties, possibly affecting its interaction with biological systems. The stereochemistry indicated by the (3aS,6S) configuration suggests specific spatial arrangements that may play a crucial role in its biological activity and interactions. Such compounds are often studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The stability, reactivity, and specific applications of this compound would depend on its functional groups and overall molecular structure, making it a subject of interest in both synthetic and medicinal chemistry.

(3aS,6S)-6-methoxy-2,2,4-trimethyl-4,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-ol

71772-35-5: The chemical substance known as (3aS,6S)-6-methoxy-2,2,4-trimethyl-4,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-ol, with the CAS number 71772-35-5, is a complex organic compound characterized by its unique bicyclic structure that incorporates a dioxole and pyran moiety. This compound features multiple methyl groups, contributing to its hydrophobic nature and potentially influencing its solubility and reactivity. The presence of a methoxy group enhances its chemical properties, possibly affecting its interaction with biological systems. The stereochemistry indicated by the (3aS,6S) configuration suggests specific spatial arrangements that may play a crucial role in its biological activity and interactions. Such compounds are often studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The stability, reactivity, and specific applications of this compound would depend on its functional groups and overall molecular structure, making it a subject of interest in both synthetic and medicinal chemistry.

Methyl 6-Deoxy-3,4-O-isopropylidene-α-D-galactopyranoside

<p>Methyl 6-deoxy-3,4-O-isopropylidene-a-D-galactopyranoside is a saccharide that has been modified by a click reaction. It is used in the synthesis of complex carbohydrates and in the modification of glycosylations. This product is manufactured using high purity reagents and can be purchased with custom synthesis options. Methyl 6-deoxy-3,4-O-isopropylidene-a-D-galactopyranoside has CAS number 71772-35-5.</p>

CAS 71772-35-5

(3aS,6S)-6-methoxy-2,2,4-trimethyl-4,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-ol

Methyl 6-Deoxy-3,4-O-isopropylidene-α-D-galactopyranoside

Ref: 7W-GC2839

Methyl 6-deoxy-3,4-O-isopropylidene-a-D-galactopyranoside

Ref: 3D-MM09722