65645-32-1 Usage
General Description
Benzenemethanamine, 4-amino-α-methyl-, (αR)-, also known as L-ephedrine, is a synthetic organic compound with a chemical structure similar to methamphetamine and amphetamine. It is commonly used as a decongestant and bronchodilator in the treatment of asthma and other respiratory conditions. L-ephedrine works by stimulating the alpha and beta adrenergic receptors, leading to the relaxation of smooth muscle in the airways and the constriction of blood vessels. It can also stimulate the central nervous system, leading to increased alertness and energy. However, L-ephedrine can also have side effects such as increased heart rate, elevated blood pressure, and nervousness, and it is regulated in many countries due to its potential for abuse and dependence.
Check Digit Verification of cas no
The CAS Registry Mumber 65645-32-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,4 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65645-32:
(7*6)+(6*5)+(5*6)+(4*4)+(3*5)+(2*3)+(1*2)=141
141 % 10 = 1
So 65645-32-1 is a valid CAS Registry Number.
65645-32-1Relevant articles and documents
COMPOUNDS FOR THE TREATMENT OF ALZHEIMER'S DISEASE
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Page/Page column 44, (2010/07/08)
The invention relates to substituted 1,2-ethylenediamines of general formula (I), wherein the radicals R1-R13, A, B, L and i are as defined in the description and in the claims. The invention also relates to the use thereof for treat
Chain-branched 1,3-dibenzylthioureas as vanilloid receptor 1 antagonists
Ryu, Chong Hyun,Jang, Mi Jung,Jung, Jeong Wha,Park, Ju-Hyun,Choi, Hye Young,Suh, Young-Ger,Oh, Uhtaek,Park, Hyeung-Geun,Lee, Jeewoo,Koh, Hyun-Joo,Mo, Joo-Hyun,Joo, Yung Hyup,Park, Young-Ho,Kim, Hee-Doo
, p. 1751 - 1755 (2007/10/03)
A series of chain-branched 1,3-dibenzylthiourea derivatives were synthesized, and tested their antagonist activity against vanilloid receptor 1. Chain-branching led to a significant change in the mode of action and the potency. (R)-Methyl or ethyl-branched 1,3-dibenzylthiourea derivatives showed the most potent antagonist activity up to the IC50 value of 0.05 μM which is 10-fold more potent than capsazepine.