1332832-16-2 Usage
General Description
(S)-1-(o-Tolyl)ethanamine hydrochloride is a chemical compound with the molecular formula C8H12ClN. It is a salt formed by the reaction of (S)-1-(o-Tolyl)ethanamine with hydrochloric acid. (S)-1-(o-Tolyl)ethanamine hydrochloride is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It has also been studied for its potential use in the treatment of certain neurological disorders. The hydrochloride salt form of (S)-1-(o-Tolyl)ethanamine is a white to off-white crystalline solid that is soluble in water and ethanol. As with any chemical, it should be handled and stored according to proper safety regulations and guidelines.
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
