112338-61-1

Basic information

• Product Name: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethyl-
• Synonyms: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethyl-
• CAS NO: 112338-61-1
• Molecular Formula: C15H17 F3 O4
• Molecular Weight: 318.29
• Mol File: 112338-61-1.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethyl-(112338-61-1)
• EPA Substance Registry System: .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethyl-(112338-61-1)

Safety Data

• Hazardous Substances Data: 112338-61-1(Hazardous Substances Data)

Usage

Description

.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethylis a complex carbohydrate compound with a unique structure. It features a ribose sugar molecule and a hexopyranose ring, along with a 1,6-anhydro-3-deoxy-2-O-methyl group and a 4-O-2-(trifluoromethyl)phenylmethyl group. This specialized molecule holds potential value in various fields, including pharmaceuticals, biochemistry, and organic chemistry, with its trifluoromethyl group offering unique properties for further research and development.

Uses

Used in Pharmaceutical Applications:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethylis used as a key component in the development of novel pharmaceutical compounds. Its unique structure and functional groups make it a promising candidate for the creation of new drugs targeting various diseases and conditions.
Used in Biochemical Research:
In the field of biochemistry, .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethylis used as a research tool to study the interactions and mechanisms of various biological processes. Its unique structure allows scientists to gain insights into the roles of carbohydrates in cellular functions and their potential applications in therapeutic strategies.
Used in Organic Chemistry:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethylis utilized in organic chemistry as a building block for the synthesis of more complex molecules. Its unique functional groups and trifluoromethyl group make it an attractive starting material for the development of new organic compounds with potential applications in various industries.
Used in Drug Delivery Systems:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-2-(trifluoromethyl)phenylmethylis also used in the development of innovative drug delivery systems. Its unique structure and properties can be exploited to improve the delivery, bioavailability, and therapeutic outcomes of various pharmaceutical agents, particularly in the context of targeted drug delivery and controlled release formulations.