1423018-01-2 Usage
Uses
Used in Pharmaceutical Research:
Ethyl thio-beta-D-galactopyranoside 2,4,6-tribenzoate is used as a synthetic intermediate for the development of complex carbohydrates and glycoconjugates, which are crucial in the formulation of new drugs and vaccines. Its role in carbohydrate chemistry is vital for understanding the biological functions and interactions of these molecules.
Used in Materials Science:
In the materials science industry, Ethyl thio-beta-D-galactopyranoside 2,4,6-tribenzoate is used as a component in the synthesis of advanced materials that leverage the unique properties of carbohydrates for various applications, including the development of new types of biomaterials.
Used in Biochemistry Research:
Ethyl thio-beta-D-galactopyranoside 2,4,6-tribenzoate is utilized as a research tool in biochemistry to study the modification and functionalization of sugar molecules. Its unique structure allows for the exploration of new biochemical pathways and the enhancement of existing ones.
Used in Organic Chemistry:
As a synthetic intermediate in organic chemistry, Ethyl thio-beta-D-galactopyranoside 2,4,6-tribenzoate is used for the synthesis of a variety of organic compounds, contributing to the advancement of organic synthesis techniques and the discovery of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 1423018-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,0,1 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1423018-01:
(9*1)+(8*4)+(7*2)+(6*3)+(5*0)+(4*1)+(3*8)+(2*0)+(1*1)=102
102 % 10 = 2
So 1423018-01-2 is a valid CAS Registry Number.
1423018-01-2Relevant academic research and scientific papers
Spijker, Nynke M.,Keuning, Cor A.,Hooglugt, Mariska,Veeneman, Gerrit H.,Van Boeckel, Constant A. A.
, p. 5945 - 5960 (1996)
The synthesis of hexasaccharide 1, [galβ(1-4)GlcNAc[6OSO3]β(1-3)Galβ(1-4)GlcNAcβ(1-3)Galβ(1-3)GalNA cα-O(CH2)3NH2], which corresponds to a porcine zona pellucida fragment that inhibits porcine sperm-oocyte interaction, is described. Compound 1 was obtained from fully protected hexasaccharide 2, which was in turn constructed from protected Galβ(1-3)GalNAc disaccharide 5, containing an α-linked 3-azidopropyl spacer, and from lactosamine derivatives 3 and 4. Disaccharide 3 and 4 were prepared by coupling of selenophenyl glycoside 6 with glycosyl acceptors containing anomeric thioethyl groups. NIS/TfOH promoted coupling of disaccharide 4 with 5 afforded 29, which was transformed into the tetrasaccharide acceptor 30 by selective removal of the levulinoyl group. Glycosylation of 30 with 3 afforded protected hexasaccharide 2. Removal of the phthalimido groups, acetylation, followed by selective removal of the allyl group and sulphation, and finally complete deprotection afforded hexasaccharide 1.
