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746551-67-7

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746551-67-7 Usage

General Description

Diethyl 2-(benzylamino)succinate is a chemical compound with the molecular formula C16H23NO4. It is a succinate derivative and contains a benzylamino group. diethyl 2-(benzylamino)succinate is used in various applications, such as in the synthesis of pharmaceuticals and agrochemicals. It is also used as an intermediate in organic synthesis and as a building block for the preparation of other chemical compounds. Diethyl 2-(benzylamino)succinate may also have potential biological activity and is of interest in the field of medicinal chemistry for its potential use in drug discovery and development. Overall, this compound has versatile uses in the chemical and pharmaceutical industries.

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.

746551-67-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-(benzylamino)succinate

1.2 Other means of identification

Product number -
Other names N-Benzyl-asparaginsaeure-diaethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:746551-67-7 SDS

746551-67-7Downstream Products

746551-67-7Relevant articles and documents

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.

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