40656-44-8 Usage
Chemical compound
6-chloro-6-deoxyglucose is a derivative of glucose, a simple sugar.
Modification
Addition of a chlorine atom at the sixth carbon position.
Biological properties
Alteration of biological properties and reactivity due to modification.
Application
Used in studies of carbohydrate metabolism and transport, as well as research for new drugs in treating metabolic disorders.
Synthesis
Useful in the synthesis of other bioactive compounds.
Potential
Valuable chemical tool in scientific and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 40656-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,5 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40656-44:
(7*4)+(6*0)+(5*6)+(4*5)+(3*6)+(2*4)+(1*4)=108
108 % 10 = 8
So 40656-44-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H11ClO5/c7-1-3(9)5(11)6(12)4(10)2-8/h2-6,9-12H,1H2/t3-,4+,5-,6-/m0/s1
40656-44-8Relevant articles and documents
FACILE PREPARATION OF DEOXYIODOCELLULOSE AND ITS CONVERSION INTO 5,6-CELLULOSENE
Ishii, Tadashi
, p. 63 - 70 (2007/10/02)
Treatment of 6-chloro-6-deoxycellulose with sodium iodide in 2,5-hexanedione gave 6-deoxy-6-iodocellulose; > 80 percent of the chlorine atoms were replaced. 6-Deoxy-6-iodo-D-glucose was identified by g.l.c.-m.s. in hydrolyzates of deoxyiodocellulose.Acetylated 6-deoxy-6-iodocellulose was converted almost quantitatively into 5,6-cellulosene acetate, wich was characterized by hydrolyzing the product and converting the resultant dicarbonyl sugar into an isopropylidene acetal 10.The changes of molecular-weight distribution during iodination and dehydroiodination were investigated by gel-permeation chromatography.
