90874-60-5 Usage
Description
2-AMINO-3',4'-DIMETHYL-ACETOPHENONE HYDROCHLORIDE is a chemical compound derived from acetophenone, featuring an amino group and two methyl groups attached to the molecule. This modification enhances its reactivity and functionality, making it a valuable building block in organic chemistry and pharmaceutical synthesis. The hydrochloride salt form of this compound improves its water solubility, broadening its range of applications.
Uses
Used in Pharmaceutical Synthesis:
2-AMINO-3',4'-DIMETHYL-ACETOPHENONE HYDROCHLORIDE is used as an intermediate in the synthesis of various pharmaceuticals due to its unique structure and reactivity. It contributes to the development of new drugs with potential therapeutic applications.
Used in Organic Compounds Synthesis:
As a versatile building block, 2-AMINO-3',4'-DIMETHYL-ACETOPHENONE HYDROCHLORIDE is used in the synthesis of a wide range of organic compounds, showcasing its utility in organic chemistry.
Used in Heterocyclic Compounds Synthesis:
2-AMINO-3',4'-DIMETHYL-ACETOPHENONE HYDROCHLORIDE is used as a building block for the synthesis of heterocyclic compounds, which possess a broad spectrum of biological activities and potential applications in various industries, including pharmaceuticals and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 90874-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,7 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90874-60:
(7*9)+(6*0)+(5*8)+(4*7)+(3*4)+(2*6)+(1*0)=155
155 % 10 = 5
So 90874-60-5 is a valid CAS Registry Number.
90874-60-5Relevant articles and documents
A Convenient Synthesis of Aminomethyl Ketones (α-Amino Ketones)
Yinglin, Han,Hongwen, Hu
, p. 615 - 618 (2007/10/02)
Several N,N-diformylaminomethyl ketones 3 were prepared by treating the respective bromomethylketone 1 with sodium diformylamide in acetonitrile at room temperature.This reaction produced from N-formylaminomethyl ketones 4 when ethanol was used as the solvent.One of the formyl groups of N,N-difomylaminomethyl ketones was selectively removed by using a catalytic amount of sodium or potassium hydroxide in alcohol to the corresponding N-formylaminomethyl ketones 4.The formyl groups of both N,N-diformyl- and N-formylaminomethyl ketones could be easily removed by either5percent hydrochloric acid in ethanol or 6N hydrochloric acid to give the corresponding aminomethyl ketone hydrochlorides 5.These reactions are general and give high yield of the products.
