52853-19-7

Basic information

• Product Name: 4-methylenemorpholin-4-ium chloride
• Synonyms: 4-methylenemorpholin-4-ium chloride
• CAS NO: 52853-19-7
• Molecular Formula: C₅H₁₀NO*Cl
• Molecular Weight: 135.592
• Mol File: 52853-19-7.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-methylenemorpholin-4-ium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methylenemorpholin-4-ium chloride(52853-19-7)
• EPA Substance Registry System: 4-methylenemorpholin-4-ium chloride(52853-19-7)

Safety Data

• Hazardous Substances Data: 52853-19-7(Hazardous Substances Data)

Upstream product

• 5625-90-1 4-(morpholinomethyl)morpholine 
• 110-91-8 morpholine 
• 50-00-0 formaldehyd 

Downstream Products

• 87177-56-8 4-hydroxy-3-morpholin-4-ylmethylbenzoic acid methyl ester 
• 28833-03-6 dichloro(1,2-dimorpholinoethane)nickel(II) 
• 562100-91-8 C₁₇H₂₂N₂O₅ 
• 562100-93-0 C₁₈H₂₄N₂O₅ 
• 562100-94-1 C₂₁H₂₂N₂O₅ 
• 562100-95-2 C₂₃H₂₆N₂O₅ 
• 10316-00-4 4-benzyl-morpholine 
• 17494-29-0 4-(4-methoxy-benzyl)-morpholine 
• 127056-93-3 5-Morpholin-4-yl-3-oxo-2-[1-phenyl-meth-(Z)-ylidene]-pentanoic acid ethyl ester; hydrochloride 
• 132090-70-1 4-<(4-Benzylamino-1,2-dihydro-1,2-dioxo-naphth-3-yl)-methyl>morpholinium-perchlorat 
• 81054-25-3 N-(4-Dimethylaminobenzyl)-N-morpholinomethyl-dimethylammoniumchlorid 
• 134045-15-1 4-<(2-Amino-1,4-dihydro-1,4-dioxo-naphth-3-yl)-methyl>-morpholiniumperchlorat 
• 134045-08-2 4--morpholiniumchlorid 
• 81054-27-5 N-(4-Dimethylaminobenzyl)-N-morpholinomethyl-pyrrolidiniumchlorid 

Relevant articles and documents

Studies on the carbenium-iminium ions derived from N-methylmorpholine-N- oxide (NMMO)

Two carbenium-iminium ions, an exo-centered species 2 and a ring-centered form 3, are derived from the widely used oxidant and cellulose solvent N-methylmorpholine-N-oxide (1) by heterolytic degradation. 3 rearranges into 2 in the presence of water, in an endothermic, bimolecular reaction involving a highly organized transition state, which is the first example of a carbenium-iminium ion interconversion. The reaction mechanism was investigated by a combined approach consisting of trapping reactions, isotopic labeling, kinetic studies, and computations on the DFT level.

Substituted Sulfonamide Compounds

Substituted sulfonamide compounds corresponding to the formula I wherein m, n, p, Q, R1, R2, R3, R4, X, Y and Z have the respective meanings defined herein, pharmaceutical compositions containing such compounds, a process for their preparation, and the use of such compounds for the treatment and/or inhibition of pain and other conditions mediated by bradykinin receptor 1 (B1R) and/or bradykinin receptor 2 (B2R).

4-oxo-4,7-dihydro-thieno[2,3-b]pyridine-5carboxamides as antiviral agents

The invention provides a compound of formula I: wherein R1, R2, R3, and R4 have any of the values defined in the specification, or a pharmaceutically acceptable salt thereof, as well as processes and intermediat