90032-83-0

Basic information

• Product Name: OTAVA-BB 7020690004
• Synonyms: 3,3,5,5-TETRAMETHYLMORPHOLIN-2-ONE;OTAVA-BB 7020690004;2-morpholinone, 3,3,5,5-tetramethyl-;3,3,5,5-Tetramethyl-2-morpholinone
• CAS NO: 90032-83-0
• Molecular Formula: C8H15NO2
• Molecular Weight: 157.212
• Mol File: 90032-83-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Density: 0.942
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: OTAVA-BB 7020690004(CAS DataBase Reference)
• NIST Chemistry Reference: OTAVA-BB 7020690004(90032-83-0)
• EPA Substance Registry System: OTAVA-BB 7020690004(90032-83-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 90032-83-0(Hazardous Substances Data)

Usage

General Description

OTAVA-BB 7020690004 is a chemical compound that belongs to the category of organic compounds known as phenylmorpholines. These are aromatic compounds containing a morpholine substituted by one or more phenyl groups. Morpholine is an organic chemical compound having a six-membered ring consisting of five carbon atoms and one nitrogen atom. More specific details regarding the properties, uses, safety measures, and potential impacts of OTAVA-BB 7020690004 are not readily available, suggesting that this chemical may be highly specialized or used primarily in niche or scientific fields.

Upstream product

• 91377-78-5 sodium 2-[2-methyl-1-hydroxy-2-propylamino]-2-methylpropionate 
• 67-66-3 chloroform 
• 124-68-5 2-Amino-2-methyl-1-propanol 
• 67-64-1 acetone 

Downstream Products

• 44982-72-1 N,N-bis(2-methyl-3-hydroxypropyl-2)amine 
• 19412-12-5 3,3,5,5-tetramethylmorpholine 

Relevant articles and documents

Continuous-Flow Synthesis and Derivatization of Aziridines through Palladium-Catalyzed C(sp3)?H Activation

A continuous-flow synthesis of aziridines by palladium-catalyzed C(sp3)?H activation is described. The new flow reaction could be combined with an aziridine-ring-opening reaction to give highly functionalized aliphatic amines through a consecutive process. A predictive mechanistic model was developed and used to design the C?H activation flow process and illustrates an approach towards first-principles design based on novel catalytic reactions.

Efficient selective oxidation of alcohols to aldehydes catalyzed by a morpholinone nitroxide

Efficient chemoselective oxidation of primary alcohols to the corresponding aldehydes is described. The transformation is promoted by a catalytic morpholinone nitroxide radical catalyst which can be easily synthesized. A broad range of substrates includin

Highly active metal-free catalysts for hydrogenation of unsaturated nitrogen-containing compounds

New highly active ansa-ammonium borate catalysts for the direct metal-free hydrogenation of imines were prepared by tuning of the basicity and steric bulkiness of their amine moieties. The highest catalytic activity among previously reported organocatalytic systems was shown for a wide range of nitrogen-containing substrates. The first example of asymmetric imine hydrogenation based on the ansa-ammonium borate concept was demonstrated. Furthermore, effective catalyst recovery by extraction of the acidic solution with an organic solvent followed by dehydration with TMSBr was elaborated. The initial findings highlight the development of more effective chiral ansa-ammonium borates for enantioselective hydrogenation. Therefore, the progress achieved in the ansa-ammonium borate concept makes it very promising for further elaboration with the aim to obtain industrially applicable catalysts. Copyright