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2,6-Piperidinedione, 1-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25115-65-5

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25115-65-5 Usage

Uses

N-Ethylglutarimide (cas# 25115-65-5) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 25115-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25115-65:
(7*2)+(6*5)+(5*1)+(4*1)+(3*5)+(2*6)+(1*5)=85
85 % 10 = 5
So 25115-65-5 is a valid CAS Registry Number.

25115-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Ethylglutarimide

1.2 Other means of identification

Product number -
Other names 1-ethylpiperidine-2,6-dione

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:25115-65-5 SDS

25115-65-5Downstream Products

25115-65-5Relevant academic research and scientific papers

Ruthenium Tetroxide Oxidation of N-Alkyllactams

Yoshifuji, Shigeyuki,Arakawa, Yukimi,Nitta, Yoshihiro

, p. 357 - 363 (2007/10/02)

Ruthenium tetroxide (RuO4) oxidation of N-alkyllactams proceeded regioselectively depending on the size of lactam ring, except for the seven-membered ring.Four- and eight-membered N-methyl- and N-ethyllactams were oxidized at the exocyclic α-carbon adjacent to nitrogen to produce the N-acyllactams and NH-lactams, while five- and six-membered lactams underwent endocyclic oxidation to yield the cyclic imides.Oxidation of seven-membered lactams yielded a mixture of products arising from both exocyclic and endocyclic oxidations.These regioselectivities were confirmed in the oxidation of substrates having a tertiary carbon at the oxidation position.Keywords---oxidation; ruthenium tetroxide oxidation; regioselective oxidation; hydroxylation; imide synthesis; N-alkyllactam; N-acyllactams; imide; ruthenium tetroxide; two-phase method

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