79337-40-9 Usage
Uses
Used in Pharmaceutical Industry:
1-Benzyl D-aspartate is used as a research compound for the development of treatments targeting neurological disorders. Its agonistic effect on NMDA receptors suggests potential applications in conditions where these receptors are implicated, such as Alzheimer's disease, Parkinson's disease, and other cognitive impairments.
Used in Cognitive Enhancement Research:
1-Benzyl D-aspartate is used as a cognitive enhancer in scientific studies, given its potential to improve learning and memory by modulating NMDA receptor activity, which is crucial for synaptic plasticity and cognitive function.
Used in Neuroprotective Studies:
1-Benzyl D-aspartate is utilized as a neuroprotective agent in research aimed at understanding and potentially mitigating neuronal damage associated with various neurological conditions. Its neuroprotective effects are under investigation to determine its capacity to shield neurons from degeneration and promote neuronal health.
Note: The uses listed are based on the potential applications derived from the compound's properties and ongoing research. The actual applications may vary as more research is conducted and as the compound's mechanisms of action are further understood.
Check Digit Verification of cas no
The CAS Registry Mumber 79337-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79337-40:
(7*7)+(6*9)+(5*3)+(4*3)+(3*7)+(2*4)+(1*0)=159
159 % 10 = 9
So 79337-40-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4/c12-9(6-10(13)14)11(15)16-7-8-4-2-1-3-5-8/h1-5,9H,6-7,12H2,(H,13,14)/t9-/m1/s1
79337-40-9Relevant articles and documents
A mild Boc deprotection and the importance of a free carboxylate
Thaqi, Ali,McCluskey, Adam,Scott, Janet L.
supporting information; experimental part, p. 6962 - 6964 (2009/04/07)
We report a facile and rapid removal of Boc protecting groups using microwave heating in H2O, with deprotection only requiring a free carboxylic acid group in the starting material. Unlike previous approaches, no additional reagents are required.