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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 recognized for its stimulant properties and is commonly utilized as a decongestant and bronchodilator in the treatment of respiratory conditions such as asthma. L-ephedrine operates by stimulating the alpha and beta adrenergic receptors, which results in the relaxation of smooth muscle in the airways and the constriction of blood vessels. Additionally, it can stimulate the central nervous system, leading to increased alertness and energy. However, due to its potential for abuse and dependence, L-ephedrine is regulated in many countries.

65645-32-1

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65645-32-1 Usage

Uses

Used in Pharmaceutical Industry:
L-ephedrine is used as a decongestant and bronchodilator for the treatment of respiratory conditions such as asthma. It is utilized for its ability to stimulate the alpha and beta adrenergic receptors, leading to the relaxation of smooth muscle in the airways and the constriction of blood vessels, which helps alleviate symptoms of respiratory distress.
Used in Central Nervous System Stimulation:
L-ephedrine is used as a stimulant for the central nervous system, which can lead to increased alertness and energy. This property makes it useful in certain medical applications where increased stimulation is required.
However, due to its potential side effects, which include increased heart rate, elevated blood pressure, and nervousness, L-ephedrine's use is carefully controlled and monitored in many countries to prevent 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.

65645-32-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-4-(1-Aminoethyl)aniline dihydrochloride

1.2 Other means of identification

Product number -
Other names 4-[(1R)-1-aminoethyl]aniline,dihydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65645-32-1 SDS

65645-32-1Relevant academic research and scientific papers

COMPOUNDS FOR THE TREATMENT OF ALZHEIMER'S DISEASE

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Page/Page column 64, (2010/06/19)

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 the claims. The invention also relates to the use thereof for treating Alzheimer's disease (AD) and similar diseases.

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.

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