The chemical substance known as b-D-Glucopyranoside, phenylmethyl 2,3,4-tris-O-(phenylmethyl)-6-O-(triphenylmethyl)-, with the CAS number 27851-28-1, is a glycoside derivative of glucose. This compound features a glucopyranoside structure, which is a six-membered cyclic form of glucose, and is modified with multiple phenylmethyl (benzyl) groups and a triphenylmethyl group. These modifications enhance its lipophilicity and stability, making it useful in various chemical applications, including organic synthesis and as a potential building block in medicinal chemistry. The presence of multiple aromatic groups can also influence its solubility and reactivity. Typically, such compounds exhibit interesting biological activities, although specific biological properties would depend on the context of their use. Additionally, the presence of multiple substituents can affect the compound's physical properties, such as melting point and solubility in different solvents. Overall, this compound represents a complex structure that combines carbohydrate chemistry with aromatic organic chemistry.

b-D-Glucopyranoside, phenylmethyl2,3,4-tris-O-(phenylmethyl)-6-O-(triphenylmethyl)-

27851-28-1: The chemical substance known as b-D-Glucopyranoside, phenylmethyl 2,3,4-tris-O-(phenylmethyl)-6-O-(triphenylmethyl)-, with the CAS number 27851-28-1, is a glycoside derivative of glucose. This compound features a glucopyranoside structure, which is a six-membered cyclic form of glucose, and is modified with multiple phenylmethyl (benzyl) groups and a triphenylmethyl group. These modifications enhance its lipophilicity and stability, making it useful in various chemical applications, including organic synthesis and as a potential building block in medicinal chemistry. The presence of multiple aromatic groups can also influence its solubility and reactivity. Typically, such compounds exhibit interesting biological activities, although specific biological properties would depend on the context of their use. Additionally, the presence of multiple substituents can affect the compound's physical properties, such as melting point and solubility in different solvents. Overall, this compound represents a complex structure that combines carbohydrate chemistry with aromatic organic chemistry.

1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-glucopyranose

<p>1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-glucopyranose is a fluorinated monosaccharide. It is synthesized by the reaction of 1,2,3,4 tetra-O-benzyl bromoacetone with sodium cyanoborohydride in sodium hydroxide solution. 1,2,3,4 Tetra-O-benzyl 6O trityl glucopyranose has been used as a glycosylation and polysaccharide modification agent for the synthesis of complex carbohydrates. This compound has also been shown to be an effective methylation agent for sugars.</p>

CAS 27851-28-1

b-D-Glucopyranoside, phenylmethyl2,3,4-tris-O-(phenylmethyl)-6-O-(triphenylmethyl)-

1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-glucopyranose

Ref: 7W-GC7103

1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-glucopyranose

Ref: 3D-MT08760