The chemical substance known as α-L-Mannopyranoside, 2-propen-1-yl 6-deoxy-3-O-(phenylmethyl)-, 2-(2-chloroacetate) is a glycoside derivative characterized by its structural complexity, which includes a pyranose ring and various functional groups. This compound features a mannopyranoside backbone, indicating it is derived from mannose, a six-carbon sugar. The presence of a 2-propen-1-yl group suggests it has unsaturation, which may impart unique reactivity, while the 6-deoxy modification indicates the absence of a hydroxyl group at the sixth carbon. The phenylmethyl (benzyl) group at the 3-O position enhances lipophilicity and may influence biological interactions. Additionally, the 2-(2-chloroacetate) moiety introduces a chloroacetate functional group, which can participate in further chemical reactions, making this compound potentially useful in synthetic organic chemistry or as a biochemical probe. Overall, this compound's unique structure may confer specific properties that could be exploited in various applications, including medicinal chemistry and carbohydrate chemistry.

a-L-Mannopyranoside, 2-propen-1-yl6-deoxy-3-O-(phenylmethyl)-, 2-(2-chloroacetate)

943307-50-4: The chemical substance known as α-L-Mannopyranoside, 2-propen-1-yl 6-deoxy-3-O-(phenylmethyl)-, 2-(2-chloroacetate) is a glycoside derivative characterized by its structural complexity, which includes a pyranose ring and various functional groups. This compound features a mannopyranoside backbone, indicating it is derived from mannose, a six-carbon sugar. The presence of a 2-propen-1-yl group suggests it has unsaturation, which may impart unique reactivity, while the 6-deoxy modification indicates the absence of a hydroxyl group at the sixth carbon. The phenylmethyl (benzyl) group at the 3-O position enhances lipophilicity and may influence biological interactions. Additionally, the 2-(2-chloroacetate) moiety introduces a chloroacetate functional group, which can participate in further chemical reactions, making this compound potentially useful in synthetic organic chemistry or as a biochemical probe. Overall, this compound's unique structure may confer specific properties that could be exploited in various applications, including medicinal chemistry and carbohydrate chemistry.

Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside

<p>Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside is a carbohydrate that belongs to the group of modified saccharides. It is a synthetic monosaccharide that can be used in the synthesis of complex carbohydrates and oligosaccharides. The fluorination at C1 position gives this compound high water solubility and improved stability. CAS No. 943307-50-4, Custom synthesis, High purity, Methylation, Glycosylation, Click modification.</p>

CAS 943307-50-4

a-L-Mannopyranoside, 2-propen-1-yl6-deoxy-3-O-(phenylmethyl)-, 2-(2-chloroacetate)

Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside

Ref: 7W-GC8454

Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside

Ref: 3D-MA07950