24332-96-5 Usage
Uses
Used in Pharmaceutical Industry:
2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride is used as a building block for the modification of biomolecules, particularly in the development of glycoconjugate drugs. Its ability to form complex carbohydrates and glycoproteins allows for the creation of new therapeutic agents with improved efficacy and reduced side effects.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride serves as a reagent in organic chemistry reactions. Its unique structure and functional groups enable the formation of various complex molecules, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride is used as a research tool in the study of carbohydrate chemistry and glycobiology. Its ability to form complex carbohydrate structures allows researchers to investigate the role of carbohydrates in biological processes and develop new strategies for targeting carbohydrate-related diseases.
Used in Diagnostics and Imaging:
2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride can be used in the development of diagnostic tools and imaging agents. Its ability to form specific carbohydrate structures can be exploited to create probes that selectively bind to target molecules, enabling the detection and imaging of various diseases and conditions.
Used in Material Science:
In the field of material science, 2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride can be used to develop new materials with unique properties. Its ability to form complex carbohydrate structures can be utilized to create self-assembling materials, hydrogels, and other advanced materials with potential applications in drug delivery, tissue engineering, and other areas.
Check Digit Verification of cas no
The CAS Registry Mumber 24332-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,3 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24332-96:
(7*2)+(6*4)+(5*3)+(4*3)+(3*2)+(2*9)+(1*6)=95
95 % 10 = 5
So 24332-96-5 is a valid CAS Registry Number.
24332-96-5Relevant academic research and scientific papers
Regioselective activation of glycosyl acceptors by a diarylborinic acid-derived catalyst
Gouliaras, Christina,Lee, Doris,Chan, Lina,Taylor, Mark S.
supporting information; experimental part, p. 13926 - 13929 (2011/10/31)
A derivative of diphenylborinic acid promotes catalytic, regioselective Koenigs-Knorr glycosylations of carbohydrate derivatives bearing multiple secondary hydroxyl groups. Robust levels of selectivity for the equatorial OH group of cis-1,2-diol motifs ar
SYNTHESIS OF FULLY AND PARTIALLY PROTECTED ALKYL 1-THIO-β-L-FUCOPYRANOSIDES
Dekany, Gyula,Ward, Peter,Toth, Istvan
, p. 227 - 236 (2007/10/02)
Fully acetylated (1d) and a mixture of partially acetylated (1a, 1b, 1c) ethyl 1-thio-β-L-fucopyranosides have been prepared in high yields from peracetylated fucopyranosyl chloride (1e) with sodium ethanethiolate/ethanethiol in 1,2-dimethoxyethane.The sa
