38440-79-8

Basic information

• Product Name: 2-Deoxy-2-fluoro-D-mannose
• Synonyms: 2-DEOXY-2-FLUORO-D-MANNOSE;2-deoxy-2-uoro-d-Mannose;(2S,3S,4R,5R)-2-fluoro-3,4,5,6-tetrahydroxyhexanal
• CAS NO: 38440-79-8
• Molecular Formula: C6H11FO5
• Molecular Weight: 182.1469432
• Product Categories: Carbohydrates & Derivatives
• Mol File: 38440-79-8.mol
• Article Data: 2

Chemical Properties

• Melting Point: 136-137 °C
• Boiling Point: 478.4 °C at 760 mmHg
• Flash Point: 243.1 °C
• Appearance: /
• Density: 1.494 g/cm³
• Vapor Pressure: 3.68E-11mmHg at 25°C
• Refractive Index: 1.505
• Storage Temp.: Hygroscopic, Store under Inert atmosphere -20°C Freezer
• Solubility: Methanol (Slightly), Water (Slightly, Sonicated)
• PKA: 12.53±0.20(Predicted)
• Stability: Very Hygroscopic
• CAS DataBase Reference: 2-Deoxy-2-fluoro-D-mannose(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Deoxy-2-fluoro-D-mannose(38440-79-8)
• EPA Substance Registry System: 2-Deoxy-2-fluoro-D-mannose(38440-79-8)

Safety Data

• Hazardous Substances Data: 38440-79-8(Hazardous Substances Data)

Usage

Description

2-Deoxy-2-fluoro-D-mannose is a chemical compound derived from D-mannose, a type of sugar. It is characterized by the replacement of a hydroxyl group with a fluorine atom at the 2-position and the absence of an oxygen atom at the 2-position. This modification gives it unique properties that make it valuable in various applications.

Uses

Used in Organic Synthesis:
2-Deoxy-2-fluoro-D-mannose is used as an intermediate in the synthesis of various organic compounds. Its unique chemical properties, including the presence of a fluorine atom and the absence of an oxygen atom at the 2-position, make it a versatile building block for creating a wide range of molecules with specific functionalities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-deoxy-2-fluoro-D-mannose is used as a starting material for the development of new drugs. Its unique structure can be exploited to design molecules with improved pharmacological properties, such as enhanced bioavailability, selectivity, and reduced side effects.
Used in Chemical Research:
2-deoxy-2-fluoro-D-mannose is also used in chemical research to study the effects of fluorination on the properties and reactivity of sugar molecules. This knowledge can be applied to develop new synthetic strategies and improve the understanding of the role of fluorine in organic chemistry.
Used in Material Science:
In material science, 2-deoxy-2-fluoro-D-mannose can be used to develop novel materials with specific properties. For example, its unique structure can be utilized to create self-assembling systems or to modify the properties of polymers and other materials.

InChI:InChI=1/C6H11FO5/c7-3(1-8)5(11)6(12)4(10)2-9/h1,3-6,9-12H,2H2/t3-,4-,5-,6-/m1/s1

Upstream product

• 84780-21-2 Fluoro-((4R,5S,4'R)-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl]-5-yl)-acetaldehyde 
• 141395-48-4 1,3,4,6-tetra-O-acetyl-2-deoxy-2-fluoro-α/β-D-glucopyranoside 

Downstream Products

• 31077-89-1 1,3,4,6-tetra-O-acetyl-2-deoxy-2-fluoro-β-D-glucopyranose 
• 7226-42-8 1,3,4,6-tetra-O-acetyl-2-deoxy-2-fluoro-α-D-glucopyranose 
• 141395-49-5 [(2R,3R,4S,5S)-3,4,6-triacetoxy-5-fluoro-tetrahydropyran-2-yl]methyl acetate 

Relevant articles and documents

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