35106-87-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-Methylphenyl)ethanamine Hydrochloride is used as a nasal decongestant for alleviating congestion and improving breathing in individuals suffering from respiratory conditions such as asthma and bronchitis. Its ability to stimulate adrenergic receptors helps in clearing nasal passages and reducing inflammation.
Used in Respiratory Treatment:
In the medical field, 1-(2-Methylphenyl)ethanamine Hydrochloride is used as a bronchodilator to treat respiratory conditions. It aids in relaxing and widening the airways, facilitating easier breathing for patients with asthma and other respiratory disorders.
Used as a Stimulant:
Due to its stimulating effects on the central nervous system, 1-(2-Methylphenyl)ethanamine Hydrochloride is used as a stimulant in over-the-counter medications. It can help increase alertness, fight fatigue, and enhance physical performance.
Regulated Substance:
Given its potential for abuse due to its stimulating effects, 1-(2-Methylphenyl)ethanamine Hydrochloride is regulated as a controlled substance in some countries. This regulation ensures that its distribution and use are monitored to prevent misuse and abuse.
Check Digit Verification of cas no
The CAS Registry Mumber 35106-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,0 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35106-87:
(7*3)+(6*5)+(5*1)+(4*0)+(3*6)+(2*8)+(1*7)=97
97 % 10 = 7
So 35106-87-7 is a valid CAS Registry Number.
35106-87-7Relevant academic research and scientific papers
Sequential reductive amination-hydrogenolysis: A one-pot synthesis of challenging chiral primary amines
Nugent, Thomas C.,Negru, Daniela E.,El-Shazly, Mohamed,Hu, Dan,Sadiq, Abdul,Bibi, Ahtaram,Umar, M. Naveed
supporting information; experimental part, p. 2085 - 2092 (2011/10/19)
Difficult-to-access chiral primary amines were formed in good to high yield and ee using a rare example of a one-pot synthesis from prochiral ketones (sequential reductive amination-hydrogenloysis). As a highlight we also demonstrate a one-pot reductive amination-hydrogenolysis-reductive amination (five reactions) of ortho-methoxyacetophenone resulting in the chiral diamine 1-(2-methoxyphenyl)ethyl-(2-pyridylmethyl)-amine (4) (58% overall yield, >99% ee), a new organocatalyst for aqueous enantioselective aldol reactions. Copyright
