122998-73-6 Usage
General Description
Trifluoroacetamidopropyl-2-acetamido-2-deoxygalactopyranoside is a synthetic chemical compound that features a trifluoroacetamide group, a propyl chain, an acetamido functional group, and a galactopyranoside structure. This unique combination of chemical groups makes trifluoroacetamidopropyl-2-acetamido-2-deoxygalactopyranoside a versatile molecule with potential applications in various fields such as pharmaceuticals, chemistry, and materials science. Its complex structure allows for interactions with biological systems, potentially enabling the development of novel drugs or materials with tailored properties. Further research and testing are needed to fully understand the potential uses and effects of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 122998-73-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,9,9 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122998-73:
(8*1)+(7*2)+(6*2)+(5*9)+(4*9)+(3*8)+(2*7)+(1*3)=156
156 % 10 = 6
So 122998-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H21F3N2O7/c1-6(20)18-8-10(22)9(21)7(5-19)25-11(8)24-4-2-3-17-12(23)13(14,15)16/h7-11,19,21-22H,2-5H2,1H3,(H,17,23)(H,18,20)/t7-,8-,9+,10-,11-/m1/s1
122998-73-6Relevant articles and documents
Synthesis of terminal disaccharide of Forssman's antigen and some of its analogs as spacered glycosides and free disaccharides
Ovchinnikova,Ter-Grigoryan,Pazynina,Bovin
, p. 55 - 68 (2007/10/03)
Spacered terminal disaccharide of Forssman's antigen GalNAcα1-3GalNAcβ1-Osp, its analog GalNAcα1-3GalNAcα1-Osp, and disaccharides Galβ1-3GalNAcβ1-Osp and Galα1-3GalNAcα1-Osp [where sp denotes the (CH2)3NHCOCF3 spacer] were synthesized. Spacered disaccharides were obtained from the (3-trifluoroacetamidopropyl)-2-acetamido-4,6-O-benzylidene-2-deoxy-β-D- galactopyranoside and its α-and β-analogs in which the 2-azido group was substituted for the 2-acetamido group. The azide glycosyl acceptors gave higher yields of the disaccharides. Azide glycosyl acceptors were prepared by the stereoselective glycosylation of 3-trifluoroacetamidopropanol with a mixture of 1-O-acetates of the 2-azido-3,4,6-tri-O-acetyl-2-deoxy-D-galactopyranose anomers in the presence of Lewis acids. Disaccharides Galα1-3GalNAc and GalNAcα1-3GalNAc were obtained from the benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-galactopyranoside.