153373-82-1 Usage
Description
.beta.-D-xylo-Hexofuranosid-5-ulose, methyl 2-(acetylamino)-2-deoxyis a chemical compound that features a methyl group attached to a sugar molecule. This sugar molecule is a derivative of the five-carbon sugar (pentose) known as Beta-D-xylo-Hexofuranosid-5-ulose, which belongs to the xylose family. Additionally, an acetylamino group is connected to a 2-deoxy sugar, a modified sugar molecule where a hydrogen atom is replaced with an acetylamino group. .beta.-D-xylo-Hexofuranosid-5-ulose, methyl 2-(acetylamino)-2-deoxyholds potential for various applications in the pharmaceutical and biotechnology sectors due to its unique structural properties and possible biological activities.
Uses
Used in Pharmaceutical Industry:
.beta.-D-xylo-Hexofuranosid-5-ulose, methyl 2-(acetylamino)-2-deoxyis used as a key compound for the development of novel drugs for various therapeutic applications. Its unique structure allows for the creation of new drug candidates that can target specific biological pathways or receptors, potentially leading to more effective treatments for a range of diseases.
Used in Biotechnology Industry:
In the biotechnology field, .beta.-D-xylo-Hexofuranosid-5-ulose, methyl 2-(acetylamino)-2-deoxycan be utilized as a building block for the synthesis of complex carbohydrates and glycoconjugates. These molecules have significant roles in cellular recognition, adhesion, and signaling processes, making them valuable for the development of new biomaterials, vaccines, and diagnostic tools.
Used in Drug Delivery Systems:
.beta.-D-xylo-Hexofuranosid-5-ulose, methyl 2-(acetylamino)-2-deoxycan also be employed in the design of drug delivery systems, where its structural properties can be exploited to improve the solubility, stability, and bioavailability of therapeutic agents. This application can lead to the development of more efficient drug formulations and targeted drug delivery approaches, ultimately enhancing the efficacy and safety of treatments.
Used in Research and Development:
.beta.-D-xylo-Hexofuranosid-5-ulose, methyl 2-(acetylamino)-2-deoxyserves as an important research tool for studying the structure and function of carbohydrates and their interactions with biological systems. This knowledge can be applied to develop a better understanding of various biological processes and the role of carbohydrates in disease development, potentially leading to the discovery of new therapeutic targets and treatment strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 153373-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,7 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 153373-82:
(8*1)+(7*5)+(6*3)+(5*3)+(4*7)+(3*3)+(2*8)+(1*2)=131
131 % 10 = 1
So 153373-82-1 is a valid CAS Registry Number.
153373-82-1Relevant articles and documents
2-Acetamido-1,2-dideoxynojirimycin: An improved synthesis
Furneaux,Gainsford,Lynch,Yorke
, p. 9605 - 9612 (2007/10/02)
The potent β-N-acetylglucosaminidase inhibitor, 2-acetamido-1,2-dideoxynojirimycin, was prepared in 6 steps from N-acetyl-D-glucosamine (overall yield 10%) via the double reductive amination of a keto aldehyde as the key step.
