4536-08-7 Usage
Uses
Used in Organic Synthesis:
6-deoxy-6-fluoro-D-glucose is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of novel molecules with potential applications in pharmaceuticals, materials science, and other chemical industries.
Used in Pharmaceutical Research:
6-deoxy-6-fluoro-D-glucose is used as a research compound for the development of new drugs. Its modified structure can be exploited to target specific biological pathways or receptors, potentially leading to the discovery of new therapeutic agents.
Used in Biochemical Studies:
As a modified sugar, 6-deoxy-6-fluoro-D-glucose can be used in biochemical research to study the effects of sugar modifications on biological processes. This can provide insights into the role of sugars in cellular metabolism and the development of diseases.
Used in Imaging and Diagnostics:
The unique chemical properties of 6-deoxy-6-fluoro-D-glucose may also make it useful in the development of imaging agents or diagnostic tools, particularly in the field of medical imaging where novel contrast agents are constantly being sought.
Used in Chemical Industry:
6-deoxy-6-fluoro-D-glucose can be utilized in the chemical industry for the production of specialty chemicals, materials, or as additives in various applications due to its distinct chemical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 4536-08-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,3 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4536-08:
(6*4)+(5*5)+(4*3)+(3*6)+(2*0)+(1*8)=87
87 % 10 = 7
So 4536-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H11FO5/c7-1-3(9)5(11)6(12)4(10)2-8/h2-6,9-12H,1H2/t3-,4+,5-,6-/m1/s1
4536-08-7Relevant academic research and scientific papers
Braun,French,Robyt
, p. 107 - 116 (1985)
Hydrolysis of 6-deoxyamylose and mono-6-deoxy-6-fluorocyclomaltoheptaose by porcine-pancreatic alpha amylase produces low-molecular-weight modified products, which have been analyzed by chemical and chromatographic techniques. Results for both substrates show that modified D-glucose and two isomers of modified maltoses are produced in the enzyme reaction. In addition, the formation of maltoses modified in the nonreducing residue is more favored than the formation of maltoses modified in the reducing residue. These results indicate that productive binding of 6-fluoro- and 6-deoxy-D-glucose residues is permitted at subsites 1 through 4 of the amylase-active site but that binding of these modified residues may be less favorable at subsite 3, the subsite at which catalytic attack occurs.
