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28833-81-0

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28833-81-0 Usage

General Description

N-ACETOXYETHYL SUCCINIMIDE is a chemical compound that belongs to the class of succinimide derivatives. It is used as a reagent in the synthesis of pharmaceutical compounds and as a modifier in the production of polymers. N-ACETOXYETHYL SUCCINIMIDE is also used in the preparation of surfactants and as a cross-linking agent in the production of resins. It has been studied for its potential use in drug delivery systems and as a chemical intermediate in the production of various organic compounds. The compound is known for its moderate toxicity and should be handled with care in laboratory and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 28833-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,3 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28833-81:
(7*2)+(6*8)+(5*8)+(4*3)+(3*3)+(2*8)+(1*1)=140
140 % 10 = 0
So 28833-81-0 is a valid CAS Registry Number.

28833-81-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,5-dioxopyrrolidin-1-yl)ethyl acetate

1.2 Other means of identification

Product number -
Other names N-(2-acetoxy-ethyl)-succinimide

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:28833-81-0 SDS

28833-81-0Relevant articles and documents

Facile synthesis of indolizinoindolone, indolylepoxypyrrolooxazole, indolylpyrrolooxazolone and isoindolopyrazinoindolone heterocycles from indole and imide derivatives

Argade, Narshinha P.,Shelar, Santosh V.

, p. 6160 - 6169 (2021/07/21)

Chemo-, regio- and diastereoselective coupling reactions of indole with imide derivatives leading to unique heterocyclic systems are demonstrated. Acid-induced 3-position coupling reactions of indole with cyclic imide derived lactamols followed by acid promoted 2-position cyclizations with the corresponding aldehydes are described to obtain the indolizinoindolones and benzoindolizinoindolones. Base induced 2-position coupling reactions ofN-tosylindole withN-(2-iodoethyl)imides and the subsequent cyclizations provide indolylepoxypyrrolooxazole, indolylpyrrolooxazolone and indolyloxazoloisoindolone. Reductive cleavage of indolyloxazoloisoindolone to the corresponding alcohol followed by mesylation and base promotedN-cyclization affords thein situair-oxidized pentacyclic product hydroxyisoindolopyrazinoindolone. A regioisomeric structural revision of the natural product from 1,2,5,6,7,11c-hexahydro-3H-indolizino[7,8-b]indol-3-one to 1,2,5,6,11,11b-hexahydro-3H-indolizino(8,7-b)indol-3-one is also reported in the present studies focussed on the methodologies for heterocyclic synthesis.

NEW CHIRAL RECOGNITION OF CHIRAL TIN(II) ENOLATES TOWARD CYCLIC ACYL IMINIUM SPECIES. ASYMMETRIC TOTAL SYNTHESIS OF (-)-SUPINIDINE

Nagao, Yoshimitsu,Dai, Wei-Min,Ochiai, Masahito

, p. 6133 - 6136 (2007/10/02)

Diastereoselective alkylation of chiral tin(II) enolates 1 onto cyclic acyl iminium ion 7 proceeded in a different chiral recognition mode from the case of 1 onto cyclic acyl imines 3.This new diastereoselective alkylation was efficiently utilized for an asymmetric total synthesis of (-)-supinidine (20).

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