101024-20-8 Usage
General Description
2-acetamido-3-S-acetyl-1,6-anhydro-4-O-benzyl-2-deoxy-3-thio-β-D-allopyranose is a complex chemical compound with a unique structure. It contains an acetamido group, an acetyl group, and a benzyl group, as well as a thioether linkage and a pyranose ring. The compound also has an anhydro bridge between the first and sixth carbon atoms, making it an anhydro sugar. Additionally, it is a derivative of 2-deoxy-β-D-allopyranose. These structural features give the chemical potential pharmaceutical and biochemical importance, as it may have applications in drug development, carbohydrate chemistry, and other fields where complex sugar derivatives are utilized.
Check Digit Verification of cas no
The CAS Registry Mumber 101024-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,2 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101024-20:
(8*1)+(7*0)+(6*1)+(5*0)+(4*2)+(3*4)+(2*2)+(1*0)=38
38 % 10 = 8
So 101024-20-8 is a valid CAS Registry Number.
101024-20-8Relevant academic research and scientific papers
REACTION OF 1,6-ANHYDRO-4-O-BENZYL-2-DEOXY-2-ISOTHIOCYANATO-β-D-GLUCOYRANOSE; PREPARATION OF 2-AMINO-1,6-ANHYDRO-2,3-DIDEOXY-β-D-ribo-HEXOPYRANOSE
Elbert, Tomas,Cerny, Miloslav
, p. 2000 - 2009 (2007/10/02)
1,6-Anhydro-4-O-benzyl-2-deoxy-2-isothiocyanato-β-D-glucopyranose (IV), prepared from 2-amino-1,6-anhydro-4-O-benzyl-2-deoxy-β-D-glucopyranose (I) by reaction with carbon disulfide followed by oxidation with iodine, was converted into the 3-O-p-toluenesulfonate VII.This was cyclized to give either the 2,3-epimino derivative X or the thiazoline XII. 2-Acetamido-3-S-acetyl-1,6-anhydro-4-O-benzyl-2-deoxy-3-thio-β-D-glucopyranose (XVI), obtained from compound XII, was desulfurized with Raney nickel to afford 2-acetamido-1,6-anhydro-2,3-dideoxy-β-D-ribo-hexopyranose (XVII).The isothiocyanato group was not affected upon acetylation of compound IV and acetolysis of the 1,6-anhydride bond with acetic anhydride and trifluoroacetic acid.
