172945-26-5 Usage
Description
HEXYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is a complex organic compound that is a derivative of glucose and belongs to the class of glycosides. It is used as a building block in organic synthesis and chemical research for creating other compounds.
Used in Organic Synthesis:
HEXYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a building block in the field of organic synthesis for creating other compounds.
Used in Chemical Research:
HEXYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a building block in chemical research for creating other compounds.
Used in Pharmaceutical Industry:
HEXYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a potential medical application in the development of new drugs and pharmaceuticals.
Used in Food Industry:
HEXYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a potential flavoring or sweetening agent in the food industry.
Check Digit Verification of cas no
The CAS Registry Mumber 172945-26-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,9,4 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 172945-26:
(8*1)+(7*7)+(6*2)+(5*9)+(4*4)+(3*5)+(2*2)+(1*6)=155
155 % 10 = 5
So 172945-26-5 is a valid CAS Registry Number.
172945-26-5Relevant articles and documents
New α-selective thermal glycosylation of acetyl-protected 2-acetamido-2-deoxy-β-D-glucopyranosyl diphenylphosphinate
Kadokawa, Jun-ichi,Nagaoka, Takeshi,Ebana, Jun,Tagaya, Hideyuki,Chiba, Koji
, p. 341 - 344 (2007/10/03)
This paper describes new α-selective thermal glycosylation using acetyl-protected 2-acetamido-2-deoxy-β-D-glucopyranosyl diphenylphosphinate (4) as a glycosyl donor. When the glycosylation of 4 with 1-hexanol was carried out under various conditions, the conditions using trimethylsilyl trifluoromethanesulfonate as a promoter in nitromethane at reflux temperature were most suitable for the formation of the α anomer. The glycosylation of 4 with the other common alcohols gave corresponding α-glycosides in relatively high yields under the conditions. When cholesterol, a very steric hindered alcohol, was used as a glycosyl acceptor, α-glycoside was also produced predominantly. Copyright (C) 2000 Elsevier Science Ltd.
Synthesis of a SLex mimic: a potential E-selectin binding antagonist
Heskamp, B. M.,Veeneman, G. H.,Marel, G. A. van der,Boeckel, C. A. A. van,Boom, J. H. van
, p. 398 - 402 (2007/10/03)
Iodonium-ion-assisted condensation of methyl 4,7,8,9-tetra-O-acetyl-N-acetyl-2-O--α-D-neuraminate (15) with hexyl 2-acetamido-6-O-benzyl-3-O-(tri-O-benzyl-α-L-fucopyranosyl)-2-deoxy-β-D-glucopyranoside (12) furnished, after de
