123919-31-3

Basic information

• Product Name: .beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethyl-
• Synonyms: .beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethyl-
• CAS NO: 123919-31-3
• Molecular Formula: C16H26O4
• Molecular Weight: 282.38
• Mol File: 123919-31-3.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethyl-(123919-31-3)
• EPA Substance Registry System: .beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethyl-(123919-31-3)

Safety Data

• Hazardous Substances Data: 123919-31-3(Hazardous Substances Data)

Usage

Description

.beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethylis a complex carbohydrate derivative featuring a heptulopyranose structure derived from ribose sugar. .beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethylis characterized by the presence of a cyclohexenylmethyl group at the 5th carbon and an ethyl group at the 3rd carbon. Additionally, it has two hydroxyl groups removed at the 2nd and 7th positions, which may contribute to its unique properties and reactivity. Given its structural complexity, it is likely to have specialized applications in the fields of biochemistry and organic chemistry.

Uses

Used in Biochemical Research:
.beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethylcan be utilized as a unique substrate or molecular probe in biochemical research. Its distinct structure may allow for the investigation of specific enzyme interactions, metabolic pathways, or cellular processes that involve heptulopyranose-containing molecules.
Used in Organic Synthesis:
In the field of organic chemistry, .beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethylmay serve as a key intermediate or building block for the synthesis of more complex organic compounds. Its unique functional groups and structural features could be exploited in the development of novel pharmaceuticals, agrochemicals, or other specialty chemicals.
Used in Drug Design:
.beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethyl-'s structural complexity and potential reactivity may make it a valuable candidate for drug design, particularly in the development of targeted therapies for various diseases. Its interaction with specific biological targets could be explored, and its modification could lead to the creation of new drugs with improved efficacy and selectivity.
Used in Material Science:
The unique structural features of .beta.-D-ribo-2-Heptulopyranose, 2,7-anhydro-5-O-(3-cyclohexen-1-ylmethyl)-1,4-dideoxy-3-O-ethylmay also find applications in material science, where it could be used to develop new materials with specific properties, such as enhanced stability, selectivity, or biocompatibility.