CAS 16977-78-9

[(3R,4S,5S,6R)-3,4,5-triacetoxy-6-(2-bromoethoxy)tetrahydropyran-2-yl]methyl acetate

Description:

The chemical substance with the name "[(3R,4S,5S,6R)-3,4,5-triacetoxy-6-(2-bromoethoxy)tetrahydropyran-2-yl]methyl acetate" and CAS number 16977-78-9 is a complex organic compound characterized by its tetrahydropyran ring structure, which is a six-membered cyclic ether. This compound features multiple acetoxy groups, indicating the presence of acetyl functional groups that enhance its reactivity and solubility in organic solvents. The presence of a bromoethoxy substituent introduces a halogen, which can participate in nucleophilic substitution reactions, making the compound potentially useful in synthetic organic chemistry. The stereochemistry, denoted by the (3R,4S,5S,6R) configuration, suggests specific spatial arrangements of atoms that can influence the compound's biological activity and interactions. Overall, this substance may exhibit interesting properties and reactivity patterns due to its functional groups and stereochemistry, making it a candidate for further study in medicinal chemistry or as a synthetic intermediate.

Formula: C₁₆H₂₃BrO₁₀

InChI: InChI=1/C16H23BrO10/c1-8(18)23-7-12-13(24-9(2)19)14(25-10(3)20)15(26-11(4)21)16(27-12)22-6-5-17/h12-16H,5-7H2,1-4H3/t12?,13-,14+,15+,16-/m1/s1

2''-Bromoethyl 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranoside

CAS: 16977-78-9

Molecular weight: 455.25

Ref: 7W-GC5296

2’-Bromoethyl 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranoside

Controlled Product

CAS: 16977-78-9

Applications 2’-Bromoethyl 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranoside (cas# 16977-78-9) is a compound useful in organic synthesis.
References Reinhard, J., et al.: J. Med. Chem., 44, 4050 (2001), Guan, L., et al.: J. Biol. Chem., 278, 10641 (2003),

Formula: C₁₆H₂₃BrO₁₀

Color and Shape: White To Off-White

Molecular weight: 455.25

Ref: TR-B684343

2-Bromoethyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside

CAS: 16977-78-9

2-Bromoethyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside is a modified form of D-(+)-glucose. The modification has been accomplished through the use of a click chemistry reaction with an azide and alkyne. This product is offered for custom synthesis and can be used in glycosylation reactions.

Formula: C₁₆H₂₃BrO₁₀

Purity: Min. 95%

Molecular weight: 455.25 g/mol

Ref: 3D-MB04521