6310-83-4 Usage
Uses
Used in Neuroscience Research:
THIQ-NOH is utilized as a research tool in neuroscience to explore its neuroprotective and anti-inflammatory properties. Its ability to modulate neurotransmitter systems makes it a valuable compound for studying the underlying mechanisms of neurodegenerative diseases.
Used in Drug Development for Neurodegenerative Diseases:
In the pharmaceutical industry, THIQ-NOH is considered a potential therapeutic agent for the treatment of neurodegenerative diseases such as Parkinson's and Alzheimer's. Its potential to modulate neurotransmitter systems suggests that it could provide neuroprotection and alleviate disease symptoms.
Used in Drug Design and Optimization:
THIQ-NOH serves as a lead compound in drug design and optimization processes. Its structure and activity can be further refined to enhance its therapeutic potential and selectivity, with the aim of developing more effective treatments for neurodegenerative conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 6310-83-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6310-83:
(6*6)+(5*3)+(4*1)+(3*0)+(2*8)+(1*3)=74
74 % 10 = 4
So 6310-83-4 is a valid CAS Registry Number.
6310-83-4Relevant academic research and scientific papers
1H and 13C studies of para-substituted benzaldoximes for evaluation of the electron donor properties of substituted amino groups
Gawinecki, Ryszard,Kolehmainen, Erkki,Kauppinen, Reijo
, p. 25 - 30 (2007/10/03)
1H and 13C NMR spectra of seventeen (E)-benzaldoximes and three acetophenone oximes, both carrying substituted p-amino groups, have been recorded and discussed from the point of view of substituent effect.The resonance effect of these substituents is not transmitted strongly to CH=NOH group.However, it is found that the chemical shift of Cpara depends linearly on ?R0 values.This dependence has been used to calculate the resonance substituent constants for the less common amino groups and the 1-pyrrolidine group is found to be the most powerful electron donor among the substituents studied.
