112338-91-7

Basic information

• Product Name: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-4-(trifluoromethyl)phenylmethyl-
• Synonyms: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-4-(trifluoromethyl)phenylmethyl-
• CAS NO: 112338-91-7
• Molecular Formula: C15H17 F3 O4
• Molecular Weight: 318.29
• Mol File: 112338-91-7.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-4-(trifluoromethyl)phenylmethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-4-(trifluoromethyl)phenylmethyl-(112338-91-7)
• EPA Substance Registry System: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-4-(trifluoromethyl)phenylmethyl-(112338-91-7)

Safety Data

• Hazardous Substances Data: 112338-91-7(Hazardous Substances Data)

Usage

Description

.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-4-(trifluoromethyl)phenylmethylis a complex sugar derivative of D-ribose, characterized by the loss of a water molecule (anhydro group), the presence of a methyl group, and a phenylmethyl group with a trifluoromethyl substituent. This chemical structure endows it with unique properties and potential interactions with biological systems, making it a promising candidate for various applications in medicinal chemistry, biochemistry, drug development, organic synthesis, and material science.

Uses

Used in Medicinal Chemistry:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-4-(trifluoromethyl)phenylmethylis used as a key intermediate for the synthesis of novel pharmaceutical compounds due to its unique structural features and potential reactivity with biological targets.
Used in Biochemistry:
In the field of biochemistry, .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-4-(trifluoromethyl)phenylmethylis used as a research tool to study the interactions between sugars and proteins or other biomolecules, which can provide insights into various biological processes and the development of new therapeutic strategies.
Used in Drug Development:
This sugar derivative is used as a potential therapeutic agent in drug development, particularly for targeting specific biological pathways or receptors that play a role in diseases. Its unique structure may allow for the design of more selective and potent drugs.
Used in Organic Synthesis:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-4-(trifluoromethyl)phenylmethylis used as a building block in organic synthesis for the creation of complex organic molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Material Science:
In material science, this sugar derivative may be utilized in the development of novel materials with specific properties, such as improved biocompatibility or enhanced interaction with biological systems, which could have applications in areas like drug delivery or tissue engineering.