956107-32-7 Usage
Uses
Used in Pharmaceutical Development:
Methyl (1-adamantyl 5-acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-2-thio-D-glycero-β-D-galacto-non-2-ylopyranosid)onate is used as a key intermediate in the synthesis of pharmaceuticals for [application reason]. Its unique structure and functional groups contribute to the development of novel drug candidates with potential therapeutic benefits.
Used in Chemical Research:
In the field of chemical research, methyl (1-adamantyl 5-acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-2-thio-D-glycero-β-D-galacto-non-2-ylopyranosid)onate is used as a model compound for studying [application reason]. Its complex structure allows researchers to explore various chemical reactions and interactions, furthering the understanding of organic chemistry and its applications.
Used in Biochemical Studies:
Methyl (1-adamantyl 5-acetamid...)onate is employed in biochemical studies as a tool compound for investigating [application reason]. Its specific structural features enable researchers to probe biological processes and mechanisms, potentially leading to new insights into the molecular basis of various diseases and conditions.
Used in Drug Delivery Systems:
In the development of drug delivery systems, methyl (1-adamantyl 5-acetamido...)onate is used as a component in the design of targeted drug carriers for [application reason]. Its chemical properties can be tailored to improve the solubility, stability, and bioavailability of therapeutic agents, enhancing their efficacy and reducing side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 956107-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,1,0 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 956107-32:
(8*9)+(7*5)+(6*6)+(5*1)+(4*0)+(3*7)+(2*3)+(1*2)=177
177 % 10 = 7
So 956107-32-7 is a valid CAS Registry Number.
956107-32-7Relevant academic research and scientific papers
Influence of side chain conformation and configuration on glycosyl donor reactivity and selectivity as illustrated by sialic acid donors epimeric at the 7-position
Kancharla, Pavan K.,Crich, David
, p. 18999 - 19007 (2014/01/06)
Two N-acetyl 4O,5N-oxazolidinone-protected sialyl thioglycosides epimeric at the 7-position have been synthesized and their reactivity and stereoselectivity in glycosylation reactions have been compared. It is demonstrated that the natural 7S-donor is bot
α-selective sialylations at -78°C in nitrile solvents with a 1-adamantanyl thiosialoside
Crich, David,Li, Wenju
, p. 7794 - 7797 (2008/03/11)
(Chemical Equation Presented) Novel 1-adamantanylthio sialosides were synthesized and coupled to acceptors under NIS/TfOH promotion conditions. These donors showed higher reactivity than the phenylthio sialosides and could be activated by NIS/TfOH in nitr
