38440-79-8 Usage
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.
Check Digit Verification of cas no
The CAS Registry Mumber 38440-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,4 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38440-79:
(7*3)+(6*8)+(5*4)+(4*4)+(3*0)+(2*7)+(1*9)=128
128 % 10 = 8
So 38440-79-8 is a valid CAS Registry Number.
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
38440-79-8Relevant academic research and scientific papers
Fluoro-substituted epipodophyllotoxin glucosides
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, (2008/06/13)
The present invention provides antitumor fluoro-substituted 4'-demethylepipodophyllotoxin glucosides.
REACTION OF 1,2-ANHYDRO-3,4:5,6-DI-O-ISOPROPYLIDENE-1-C-NITRO-D-MANNITOL WITH POTASSIUM HYDROGENEFLUORIDE IN ETHYLENE GLYCOL: A SYNTHESIS OF 2-DEOXY-2-FLUORO-D-GLUCOSE
Szarek, Walter A.,Hay, George W.,Doboszewski, Bogdan,Perlmutter, Milton M.
, p. 107 - 118 (2007/10/02)
The reaction of 1,2-anhydro-3,4:4,5-di-O-isopropylidene-1-C-nitro-D-mannitol (2) with potassium hydrogenfluoride in ethylene glycol under anhydrous conditions provides a route to 2-deoxy-2-fluoro-D-glucose, the (18)F-labeled analog of which is an important radiopharmaceutical of use in medical imaging.The reaction is accompained to a minor extent by epimerization at C-2 of the initially formed fluoro aldehyde and also results in attack by solvent at C-2 in 2.
