53773-37-8 Usage
Primary Use
Intermediate in the production of pharmaceuticals and organic compounds
Physical Form
White to off-white powder
Melting Point
Approximately 198-202°C
Derivative
Derived from 1-acetonaphthone
Reactivity
Exhibits reactivity in organic synthesis
Industry Application
Widely used in the pharmaceutical industry
Synthesis Role
Functions as a building block for various heterocycles
Heterocycles
Essential components in the development of therapeutic drugs and medicinal compounds
Biological Studies
Subject of research for potential biological activities
Pharmacological Properties
Investigated for its pharmacological effects
Check Digit Verification of cas no
The CAS Registry Mumber 53773-37-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,7 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53773-37:
(7*5)+(6*3)+(5*7)+(4*7)+(3*3)+(2*3)+(1*7)=138
138 % 10 = 8
So 53773-37-8 is a valid CAS Registry Number.
53773-37-8Relevant academic research and scientific papers
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.
