935-43-3 Usage
Uses
Used in Pharmaceutical Research and Development:
(Phenylcyclopropyl)methylamine Hydrochloride is used as a research compound for its analgesic and anti-inflammatory properties, as well as its potential role in modulating serotonin and dopamine levels in the brain. This makes it a promising candidate for the development of treatments for psychiatric and neurological disorders, including depression and other mood disorders.
Used in Enzyme Inhibition:
(Phenylcyclopropyl)methylamine Hydrochloride is used as a potent inhibitor of the enzyme monoamine oxidase, which plays a crucial role in the breakdown of neurotransmitters such as serotonin, dopamine, and norepinephrine. By inhibiting this enzyme, the compound may help in the treatment of certain psychiatric and neurological disorders where monoamine oxidase activity is implicated.
Used in Modulating Neurotransmitter Levels:
(Phenylcyclopropyl)methylamine Hydrochloride is used to modulate the levels of serotonin and dopamine in the brain, which are neurotransmitters that play a significant role in mood regulation, motivation, and cognitive function. This property makes it a potential candidate for the development of treatments for depression and other mood disorders where an imbalance in these neurotransmitters is observed.
Check Digit Verification of cas no
The CAS Registry Mumber 935-43-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 935-43:
(5*9)+(4*3)+(3*5)+(2*4)+(1*3)=83
83 % 10 = 3
So 935-43-3 is a valid CAS Registry Number.
935-43-3Relevant academic research and scientific papers
Chan, Kelvin S. L.,Fu, Hai-Yan,Yu, Jin-Quan
, p. 2042 - 2046 (2015)
C-H arylation via a Pd(II)/Pd(IV) catalytic cycle has been one of the most extensively studied C-H activation reactions since the 1990s. Despite the rapid development of this reaction in the past two decades, an enantioselective version has not been reported to date. Herein, we report a Pd(II)-catalyzed highly enantioselective (up to 99.5% ee) arylation of cyclopropyl C-H bonds with aryl iodides using mono-N-protected amino acid (MPAA) ligands, providing a new route for the preparation of chiral cis-aryl-cyclopropylmethylamines. The enantiocontrol is also shown to override the diastereoselectivity of chiral substrates.
