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4-(4-MORPHOLINO) ETHYL PYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 28487-18-5 Structure
  • Basic information

    1. Product Name: 4-(4-MORPHOLINO) ETHYL PYRIDINE
    2. Synonyms: 4-(4-MORPHOLINO) ETHYL PYRIDINE
    3. CAS NO:28487-18-5
    4. Molecular Formula: C11H16N2O
    5. Molecular Weight: 192.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 28487-18-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(4-MORPHOLINO) ETHYL PYRIDINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-MORPHOLINO) ETHYL PYRIDINE(28487-18-5)
    11. EPA Substance Registry System: 4-(4-MORPHOLINO) ETHYL PYRIDINE(28487-18-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 28487-18-5(Hazardous Substances Data)

28487-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28487-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,8 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28487-18:
(7*2)+(6*8)+(5*4)+(4*8)+(3*7)+(2*1)+(1*8)=145
145 % 10 = 5
So 28487-18-5 is a valid CAS Registry Number.

28487-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-MORPHOLINO) ETHYL PYRIDINE

1.2 Other means of identification

Product number -
Other names 4-[2-(4-Pyridinyl)Ethyl]Morpholine

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:28487-18-5 SDS

28487-18-5Relevant articles and documents

Aza-Michael-type addition reaction catalysed by a supported ionic liquid phase incorporating an anionic heteropoly acid

Ghasemi, Mohammad Hadi,Kowsari, Elaheh,Shafiee, Abbas

, p. 1150 - 1153 (2016/03/09)

In this work, we have obtained substituted amines under mild conditions in good yields using the Aza-Michael-type addition of various amines to vinyl compounds catalysed by a supported ionic liquid incorporating an anionic heteropoly acid. Different catalysts, including Lewis acids, Br?nsted acids and heteropoly acids were investigated in which heteropoly acids having dual Br?nsted and Lewis acid characteristics were excellent catalysts. The ionic liquid incorporating a polytungstate anion supported on magnetic diatomaceous earth as a magnetically separable heterogeneous catalyst offered the best results in terms of yield. The solid nanocatalyst was easily removed with a magnet.

Lewis acid activation of pyridines for nucleophilic aromatic substitution and conjugate addition

Abou-Shehada, Sarah,Teasdale, Matthew C.,Bull, Steven D.,Wade, Charles E.,Williams, Jonathan M. J.

, p. 1083 - 1087 (2015/03/30)

A clean, mild and sustainable method for the functionalization of pyridines and their analogues is reported. A zinc-based Lewis acid is used to activate pyridine and its analogues towards nucleophilic aromatic substitution, conjugate addition, and cyclization reactions by binding to the nitrogen on the pyridine ring and activating the pyridine ring core towards further functionalization.

Benzenesulphonamide derivatives, method for production and use thereof for treatment of pain

-

Page/Page column 18, (2008/06/13)

The present invention concerns novel benzenesulphonamide compounds, defined by formula I and the description, their method of preparation and their use in therapy.

Anti-Markonikov reactions, 6. Rhodium-catalyzed amination of vinylpyridines: Hydroamination versus oxidative amination

Beller, Matthias,Trauthwein, Harald,Eichberger, Martin,Breindl, Claudia,Mueller, Thomas E.

, p. 1121 - 1132 (2007/10/03)

Cationic rhodium complexes catalyze the amination of 2- and 4- vinylpyridine with secondary amines. Depending on the substrate and the reaction conditions either oxidative amination to yield the corresponding enamines 1a-8a or hydroamination to give 2-aminoethylpyridines 1b-8b occurs. In all cases products with anti-Markovnikov regioselectivity are obtained. For mechanistic studies novel cationic complexes of rhodium(I)-containing cyclooctadiene and vinylpyridine 12 as well as complexes containing cyclooctadiene, vinylpyridine, and morpholine 13 were prepared and characterized by NMR spectroscopy and X-ray diffraction analysis.

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