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Methylene-morpholin-4-yl-amine is a chemical compound with the molecular formula C6H14N2O. It is a derivative of morpholine, an organic heterocyclic compound consisting of a six-membered ring with two oxygen atoms and two nitrogen atoms. methylene-morpholin-4-yl-amine is characterized by the presence of a methylene group (-CH2-) attached to the morpholine ring, which is further connected to an amino group (-NH2). Methylene-morpholin-4-yl-amine is used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique reactivity and stability. It is also known for its potential applications in the development of new materials and as a catalyst in various chemical reactions.

5824-79-3

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5824-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5824-79-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5824-79:
(6*5)+(5*8)+(4*2)+(3*4)+(2*7)+(1*9)=113
113 % 10 = 3
So 5824-79-3 is a valid CAS Registry Number.

5824-79-3Relevant academic research and scientific papers

HYDROXY-, ALKOXY-, AMINOMETHYLATION OF NH-OXAZIRIDINES

Varlamov, S. V.,Kadorkina, G. K.,Kostyanovskii, R. G.

, p. 320 - 325 (1988)

3,3-Dimethyloxaziridine reacts with chloral and acetaldehyde to give crystalline N-(α-hydroxyalkyl)oxaziridines; the reaction with acetaldehyde is reversible.The N-aminomethylation of NH-oxaziridines is not realized, evidently because of the tendency of oxaziridines to iminate nucleophiles.The weakly nucleophilic chloromethylphthalimide and chloromethyl methyl ether give imidomethyl- and methoxymethyloxaziridines. 3,3-Dimethyldiaziridine reacts with excess chloromethyl methyl eter to give the N-monomethoxymethyl derivative.It is shown that α-hydroxyalkyloxaziridines and methoxymethyl-substituted oxaziridine and dizaridine do not enter into the aminomethylation of compounds with a labile hydrogen.

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