480444-13-1 Usage
Description
(S)-2-(+)-AMINO-3,3-DIMETHYL-1,1-DIPHENYLBUTANE, commonly known as dextroamphetamine, is a central nervous system stimulant with a chemical structure that features a chiral carbon atom, giving it a specific stereochemistry. It is characterized by its ability to increase the levels of certain neurotransmitters in the brain, which in turn affects attention, behavior, energy, alertness, mood, and appetite.
Uses
Used in Pharmaceutical Industry:
Dextroamphetamine is used as a therapeutic agent for treating attention deficit hyperactivity disorder (ADHD) and narcolepsy. It functions by increasing the levels of dopamine and norepinephrine in the brain, which are neurotransmitters crucial for controlling attention and behavior. This enhancement in neurotransmitter levels helps improve focus, reduce impulsivity, and manage hyperactivity in individuals with ADHD. Additionally, it is used to promote wakefulness in patients suffering from narcolepsy.
Used in Research and Development:
In the field of neuroscience and pharmacology, dextroamphetamine is utilized as a research compound to study the effects of central nervous system stimulants on neurotransmitter release and uptake, as well as their impact on cognitive function and behavior. This helps in understanding the underlying mechanisms of ADHD and other related conditions, and in the development of new treatments and medications.
Check Digit Verification of cas no
The CAS Registry Mumber 480444-13-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,0,4,4 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 480444-13:
(8*4)+(7*8)+(6*0)+(5*4)+(4*4)+(3*4)+(2*1)+(1*3)=141
141 % 10 = 1
So 480444-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H23N/c1-18(2,3)17(19)16(14-10-6-4-7-11-14)15-12-8-5-9-13-15/h4-13,16-17H,19H2,1-3H3/t17-/m0/s1
480444-13-1Relevant articles and documents
Simple primary β-amino alcohol catalyzed enantioselective Diels-Alder reaction of 3-hydroxy-2-pyridones
Takahashi, Toshihisa,Subba Reddy,Kohari, Yoshihito,Seki, Chigusa,Furuyama, Taniyuki,Kobayashi, Nagao,Okuyama, Yuko,Kwon, Eunsang,Uwai, Koji,Tokiwa, Michio,Takeshita, Mitsuhiro,Nakano, Hiroto
, p. 5771 - 5776 (2016/12/03)
The simple primary β-amino alcohol catalyzed Diels-Alder reaction of 3-hydroxy-2-pyridones as dienes with N-substituted maleimides to provide the highly substituted optically active isoquinuclidines as a single diastereomers in excellent enantioselectivities (up to 98%) with excellent chemical yields (up to 95%) was demonstrated. A range of simple β-amino alcohols were synthesized from the corresponding inexpensive amino acids and their catalytic activity was examined for this reaction.