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2-ethyl-4-methoxy-6-(morpholin-4-yl)-1,3,5-triazine is a complex organic compound with the molecular formula C10H16N4O2. It features a triazine ring, which is a six-membered aromatic ring containing three nitrogen atoms, with a 2-ethyl group attached to one of the carbon atoms, a 4-methoxy group (-OCH3) attached to another carbon atom, and a morpholin-4-yl group (a morpholine ring with a nitrogen atom) attached to the remaining carbon atom. 2-ethyl-4-methoxy-6-(morpholin-4-yl)-1,3,5-triazine is known for its potential applications in various chemical and pharmaceutical industries, particularly as a building block for the synthesis of other compounds or as a chemical intermediate. Its specific properties and reactivity make it a valuable component in the development of new materials and drugs.

5248-51-1

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5248-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5248-51-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,4 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5248-51:
(6*5)+(5*2)+(4*4)+(3*8)+(2*5)+(1*1)=91
91 % 10 = 1
So 5248-51-1 is a valid CAS Registry Number.

5248-51-1SDS

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 4-(4-ethyl-6-methoxy-1,3,5-triazin-2-yl)morpholine

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5248-51-1 SDS

5248-51-1Downstream Products

5248-51-1Relevant academic research and scientific papers

Trizaine-based dehydrative condensation reagents bearing carbon-substituents

Kitamura, Masanori,Komine, Sayaka,Kunishima, Munetaka,Yamada, Kohei

, (2020/02/22)

Herein, we report on the synthesis of alkyl-, aryl-, and alkynyl-substituted chlorotriazines and their ammonium salts, and demonstrate their utility in dehydrative condensation reactions. Although the electrophilicity of these reagents is mainly dependent on the hybridization of the carbon-substituents, it was found that bulky 2,6-dimethylphenyl group-substituted reagents resulted in the highest product yields because of a slight increase in reagent electrophilicity and/or steric hindrance favorable for desired dehydrative condensation reactions.

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