1332832-16-2 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
(S)-1-(o-Tolyl)ethanamine hydrochloride is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a versatile component in the creation of new and existing compounds, enhancing their efficacy and applicability in the medical and agricultural fields.
Used in Neurological Disorder Treatment Research:
(S)-1-(o-Tolyl)ethanamine hydrochloride is used as a potential therapeutic agent in the research and development of treatments for certain neurological disorders. Its specific properties are being studied to understand its potential impact on the nervous system and its ability to alleviate symptoms or treat the underlying conditions of these disorders.
In the context of different industries, the applications may be further specified as follows:
Used in Pharmaceutical Industry:
(S)-1-(o-Tolyl)ethanamine hydrochloride is used as a chemical intermediate for the synthesis of drugs, contributing to the development of new medications that address a range of health conditions.
Used in Agrochemical Industry:
(S)-1-(o-Tolyl)ethanamine hydrochloride is used as a building block in the formulation of agrochemicals, such as pesticides and herbicides, to improve crop protection and yield.
It is important to handle and store (S)-1-(o-Tolyl)ethanamine hydrochloride according to proper safety regulations and guidelines to ensure the safety of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 1332832-16-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,8,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1332832-16:
(9*1)+(8*3)+(7*3)+(6*2)+(5*8)+(4*3)+(3*2)+(2*1)+(1*6)=132
132 % 10 = 2
So 1332832-16-2 is a valid CAS Registry Number.
1332832-16-2Relevant articles and documents
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
, 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
