23094-81-7 Usage
Structure
Hexose ring with four acetyl groups and a phenylamino-thiol group attached.
The compound consists of a six-carbon sugar ring with additional functional groups.
Usage
Organic chemistry research and pharmaceutical development
The compound is commonly used in these fields due to its potential biological activity and reactivity.
Synthesis
Building block for the creation of more complex compounds
It can be employed in the synthesis of various carbohydrate-based molecules.
Thiohexopyranose structure
Target for the development of new drugs and therapeutic agents
The unique structure of the compound makes it a promising candidate for the development of novel pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 23094-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,9 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23094-81:
(7*2)+(6*3)+(5*0)+(4*9)+(3*4)+(2*8)+(1*1)=97
97 % 10 = 7
So 23094-81-7 is a valid CAS Registry Number.
23094-81-7Relevant articles and documents
Novel approaches to the syntheses of N-substituted S-glycosyl-sulfenamides
Illyes, Tuende-Zita,Molnar-Gabor, Dora,Szilagyi, Laszlo
, p. 1561 - 1564 (2007/10/03)
Bis(tetra-O-acetyl-β-D-glucopyranosyl)disulfide reacts, under silver ion activation, with primary and secondary aliphatic as well as aromatic amines to furnish the title compounds in moderate to good yields. The same derivatives could also be obtained fro
