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3518-88-5

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3518-88-5 Usage

General Description

Diethyl 3,3'-iminodipropionate is a chemical compound with the molecular formula C11H21NO4. It is used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Diethyl 3,3'-IMinodipropionate has two ester groups, which makes it a versatile building block for various organic syntheses. Diethyl 3,3'-iminodipropionate is also commonly used as a chiral building block in the production of chiral drugs and for the preparation of chiral ligands in asymmetric catalysis. It is a white to off-white crystalline solid and has a relatively low toxicity, making it a valuable and widely-used chemical in the pharmaceutical and agricultural industries.

Check Digit Verification of cas no

The CAS Registry Mumber 3518-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3518-88:
(6*3)+(5*5)+(4*1)+(3*8)+(2*8)+(1*8)=95
95 % 10 = 5
So 3518-88-5 is a valid CAS Registry Number.

3518-88-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-[(3-ethoxy-3-oxopropyl)amino]propanoate

1.2 Other means of identification

Product number -
Other names 3,3'-iminobis(ethyl propionate)

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:3518-88-5 SDS

3518-88-5Relevant articles and documents

On the Virtue of Indium in Reduction Reactions. A Comparison of Reductions Mediated by Indium and Zinc: Is Indium Metal an Effective Catalyst for Zinc Induced Reductions?

Matassini, Camilla,Bonanni, Marco,Marradi, Marco,Cicchi, Stefano,Goti, Andrea

supporting information, p. 1106 - 1113 (2019/12/24)

Indium(0)-mediated reductions have been reported for the transformation of several functional groups (imines, oximes, nitro groups, isoxazolidines, and conjugated alkenes, among others), prompted by the opportunity of performing the reactions in aqueous media and green conditions. We describe here the comparison of several reactions using indium or the less expensive zinc, carried out in order to evaluate the effective advantages brought about indium metal. We found some reactions for which use of In is mandatory and others where Zn worked equally well or even better. The reduction of hydroxylamines to the corresponding amines was the only reduction for which use of In provided much better results than Zn and was also possible to apply an efficient catalytic version with use of 2–5 mol-% In in the presence of stoichiometric Zn. Applicability of this catalytic reduction to “one-pot” model processes is also demonstrated.

Synthesis method of bacterial infection resistant medicine intermediate

-

Paragraph 0026; 0034; 0035, (2018/07/30)

The invention belongs to the technical field of chemical medicine intermediate synthesis, and particularly relates to a synthesis method of a bacterial infection resistant medicine intermediate. Liquid ammonia and acrylic ester are used as raw materials for preparing a diester type secondary amine compound 1; then, through cyclization, piperidone is prepared; then, scientific reaction catalysts, temperature and time are used; substitution reaction of secondary amine and iso-propyl iodide is used; the target product is synthesized through six-step reaction; the yield of the whole route reachesup to 35 percent.

Mild and Selective Cobalt-Catalyzed Chemodivergent Transfer Hydrogenation of Nitriles

Shao, Zhihui,Fu, Shaomin,Wei, Mufeng,Zhou, Shaolin,Liu, Qiang

supporting information, p. 14653 - 14657 (2016/11/23)

Herein, we describe a selective cobalt-catalyzed chemodivergent transfer hydrogenation of nitriles to synthesize primary, secondary, and tertiary amines. The solvent effect plays a key role for the selectivity control. The general applicability of this procedure was highlighted by the synthesis of more than 70 amine products bearing various functional groups in high chemoselectivity. Moreover, this mild system achieved >2000 TONs (turnover numbers) for the transfer hydrogenation of nitriles.

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