71031-17-9 Usage
Uses
Used in Pharmaceutical Industry:
R-Modafinil is used as a treatment for sleep disorders such as narcolepsy, sleep apnea, and shift work sleep disorder. It promotes wakefulness and alertness by affecting the neurotransmitters in the brain, providing relief for individuals suffering from these conditions.
Used in Cognitive Enhancement:
R-Modafinil is used as a cognitive enhancer to improve focus, attention, and overall cognitive function. Its potential cognitive enhancing effects make it a subject of interest for individuals seeking to improve their mental performance.
Used in Neuroprotection:
R-Modafinil is used for its potential neuroprotective effects, which may help protect the brain from damage or degeneration. This application is still under investigation, but it holds promise for future therapeutic applications in neurodegenerative diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 71031-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,3 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71031-17:
(7*7)+(6*1)+(5*0)+(4*3)+(3*1)+(2*1)+(1*7)=79
79 % 10 = 9
So 71031-17-9 is a valid CAS Registry Number.
71031-17-9Relevant academic research and scientific papers
New synthetic strategy for high-enantiopurity N-protected α-amino ketones and their derivatives by asymmetric hydrogenation
Sun, Tian,Hou, Guohua,Ma, Miaofeng,Zhang, Xumu
, p. 253 - 256 (2011/04/16)
Asymmetric hydrogenation of α-dehydroamino ketones catalyzed by a rhodium-chiral phosphorus ligand complex (up to 99% ee, 1000 TON), represents an efficient approach to chiral α-amino ketones. The reduction of α-amino ketones catalyzed by palladium on carbon (Pd/C) leads to amphetamine precursors with quantitative yield and no significant enantioselectivity loss.
Rapid synthesis of oxazoles under microwave conditions
Brain, Christopher T.,Paul, Jane M.
, p. 1642 - 1644 (2007/10/03)
A new and efficient variation of the Robinson-Gabriel oxazole synthesis is described. Oxazoles were prepared by cyclodehydration of 2-acylamino carbonyl compounds with Burgess reagent under monomode microwave irradiation.
