α-D-Mannopyranoside, 4-nitrophenyl 4,6-O-(phenylmethylene)-, 2-benzoate, (R)- (9CI) is a complex carbohydrate derivative characterized by its structural components and functional groups. This compound features a mannopyranoside backbone, which is a six-membered cyclic form of mannose, a type of sugar. The presence of the 4-nitrophenyl group indicates that it has a nitro substituent, which can enhance its reactivity and solubility in organic solvents. The 4,6-O-(phenylmethylene) modification suggests that the hydroxyl groups at positions 4 and 6 are protected by a phenylmethylene group, which can influence the compound's stability and reactivity. Additionally, the 2-benzoate moiety indicates that a benzoate group is attached at the second carbon, contributing to the compound's overall hydrophobic character. The (R) configuration denotes the specific stereochemistry at the chiral centers, which can affect biological activity and interactions. Overall, this compound is likely to be used in biochemical applications, particularly in glycosylation reactions or as a substrate for enzyme studies.

a-D-Mannopyranoside, 4-nitrophenyl4,6-O-(phenylmethylene)-, 2-benzoate, (R)- (9CI)

94063-92-0: α-D-Mannopyranoside, 4-nitrophenyl 4,6-O-(phenylmethylene)-, 2-benzoate, (R)- (9CI) is a complex carbohydrate derivative characterized by its structural components and functional groups. This compound features a mannopyranoside backbone, which is a six-membered cyclic form of mannose, a type of sugar. The presence of the 4-nitrophenyl group indicates that it has a nitro substituent, which can enhance its reactivity and solubility in organic solvents. The 4,6-O-(phenylmethylene) modification suggests that the hydroxyl groups at positions 4 and 6 are protected by a phenylmethylene group, which can influence the compound's stability and reactivity. Additionally, the 2-benzoate moiety indicates that a benzoate group is attached at the second carbon, contributing to the compound's overall hydrophobic character. The (R) configuration denotes the specific stereochemistry at the chiral centers, which can affect biological activity and interactions. Overall, this compound is likely to be used in biochemical applications, particularly in glycosylation reactions or as a substrate for enzyme studies.

4-Nitrophenyl 2-benzoyl-4,6-O-benzylidene-a-D-mannopyranoside

<p>4-Nitrophenyl 2-benzoyl-4,6-O-benzylidene-a-D-mannopyranoside is a glycosylated sugar that has been modified with methyl groups and fluorine atoms. It is a synthetic, monosaccharide oligosaccharide that can be custom synthesized to suit your needs. This product is CAS No. 94063-92-0 and it is available in high purity.</p>

CAS 94063-92-0

a-D-Mannopyranoside, 4-nitrophenyl4,6-O-(phenylmethylene)-, 2-benzoate, (R)- (9CI)

4-Nitrophenyl 2-benzoyl-4,6-O-benzylidene-a-D-mannopyranoside

Ref: 7W-GC6857

4-Nitrophenyl 2-benzoyl-4,6-O-benzylidene-a-D-mannopyranoside

Ref: 3D-MN05350