746551-67-7 Usage
Uses
Used in Pharmaceutical Industry:
Diethyl 2-(benzylamino)succinate is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs, potentially leading to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, diethyl 2-(benzylamino)succinate serves as a crucial building block for the synthesis of agrochemicals. Its versatility in chemical reactions enables the creation of new compounds with potential applications in agriculture, such as pesticides and herbicides.
Used in Organic Synthesis:
As an intermediate in organic synthesis, diethyl 2-(benzylamino)succinate is utilized for the preparation of other chemical compounds. Its reactivity and functional groups make it a valuable component in the synthesis of a wide range of organic molecules.
Used in Medicinal Chemistry:
Diethyl 2-(benzylamino)succinate is of interest in the field of medicinal chemistry due to its potential biological activity. Researchers are exploring its potential use in drug discovery and development, with the aim of identifying new therapeutic agents that can be used to treat various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 746551-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,6,5,5 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 746551-67:
(8*7)+(7*4)+(6*6)+(5*5)+(4*5)+(3*1)+(2*6)+(1*7)=187
187 % 10 = 7
So 746551-67-7 is a valid CAS Registry Number.
746551-67-7Relevant academic research and scientific papers
Base-promoted c→n acyl rearrangement: An unconventional approach to α-amino acid derivatives
Ugarriza, Iratxe,Uria, Uxue,Carrillo, Luisa,Vicario, Jose L.,Reyes, Efraim
, p. 11650 - 11654 (2014/10/15)
We have discovered that N-alkyl aminomalonates undergo a fast and selective intramolecular C→N acyl rearrangement reaction in the presence of a strong base, leading to N-protected glycinates in excellent yield. Moreover, the fact that the reaction proceeds through a nucleophilic enolate intermediate has been used for implementing a tandem rearrangement/alkylation sequence that has been applied to the preparation of synthetically relevant nonproteinogenic tertiary and quaternary N-alkyl α-amino acids in a very simple and reliable way.
