112338-84-8

Basic information

• Product Name: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methyl-
• Synonyms: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methyl-
• CAS NO: 112338-84-8
• Molecular Formula: C14H17 Br O4
• Molecular Weight: 329.19
• Mol File: 112338-84-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methyl-(112338-84-8)
• EPA Substance Registry System: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methyl-(112338-84-8)

Safety Data

• Hazardous Substances Data: 112338-84-8(Hazardous Substances Data)

Usage

Description

.beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methylis a unique chemical compound that features a ribose sugar molecule with a distinctive structural composition. The ribose sugar is in the beta configuration and adopts a pyranose form, characterized by a six-membered ring structure. .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methylalso includes a 1,6-anhydro-3-deoxy group and a 2-bromophenylmethyl group attached to the fourth carbon, along with a methyl group at the second carbon. The presence of these functional groups may endow the compound with specific biological activities or properties, making it a promising candidate for research in medicinal chemistry, bioconjugation, and carbohydrate chemistry.

Uses

Used in Medicinal Chemistry:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methylis used as a key building block for the synthesis of various biologically active molecules in medicinal chemistry. .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methyl-'s unique structure, including the 2-bromophenylmethyl and methyl groups, can be exploited to design and develop novel drugs with potential therapeutic applications.
Used in Bioconjugation:
In the field of bioconjugation, .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methylserves as a versatile linker or scaffold for the attachment of biologically relevant molecules, such as proteins, peptides, or other small molecules. .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methyl-'s structural features facilitate the formation of stable conjugates, which can be utilized in various biotechnological and pharmaceutical applications.
Used in Carbohydrate Chemistry Research:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methylis employed as a valuable research tool in carbohydrate chemistry. .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methyl-'s distinct structural elements, such as the 1,6-anhydro-3-deoxy group and the pyranose ring, make it an attractive candidate for studying the synthesis, modification, and biological recognition of carbohydrates. This research can lead to a deeper understanding of carbohydrate-mediated biological processes and the development of new carbohydrate-based therapeutics.
Used in Drug Delivery Systems:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methyl.beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methylcan be utilized in the development of innovative drug delivery systems. Its unique structural features can be exploited to enhance the solubility, stability, and bioavailability of therapeutic agents, leading to improved drug efficacy and reduced side effects. .beta.-D-ribo-Hexopyranose, 1,6-anhydro-4-O-(2-bromophenyl)methyl-3-deoxy-2-O-methylcan be incorporated into various drug delivery platforms, such as nanoparticles, liposomes, or hydrogels, to achieve targeted and controlled drug release.