88933-19-1

Basic information

• Product Name: Benzenamine, N-(methoxymethyl)-
• CAS NO: 88933-19-1
• Molecular Formula: C8H11NO
• Molecular Weight: 137.181
• Mol File: 88933-19-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-(methoxymethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-(methoxymethyl)-(88933-19-1)
• EPA Substance Registry System: Benzenamine, N-(methoxymethyl)-(88933-19-1)

Safety Data

• Hazardous Substances Data: 88933-19-1(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 50-00-0 formaldehyd 
• 62-53-3 aniline 
• 124-41-4 sodium methylate 
• 100-61-8 N-methylaniline 
• 109-87-5 Dimethoxymethane 

Downstream Products

• 121194-55-6 N,N-Diethyl-N'-phenyl-but-2-yne-1,4-diamine 
• 84257-36-3 (N-phenyl)aminomethylcyclopentane 
• 1126-78-9 N-(n-butyl)aniline 
• 100-62-9 N-methylenebenzenamine 
• 100-61-8 N-methylaniline 
• 91-78-1 1,3,5-triphenylhexahydro-1,3,5-triazine 
• 491-35-0 C₆H₄NCH₂CHCCH₂ 
• 90921-20-3 allenylmethylaniline 
• 205676-18-2 4-methylene-1,2,3,4-tetrahydroquinoline 
• 101-77-9 4,4'-diamino diphenyl methane 
• 121194-57-8 N-Phenyl-N'-m-tolyl-but-2-yne-1,4-diamine 
• 14130-04-2 1,4-dianilino-2-butyne 
• 2655-27-8 N-pentylaniline 
• 147454-97-5 ethyl N-phenylaziridine-2-carboxylate 

Relevant articles and documents

Tracing and elucidating visible-light mediated oxidation and C-H functionalization of amines using mass spectrometry

The co-existing mechanism of visible light mediated direct oxidation and C-H functionalization of amines was investigated by capturing all the intermediates using online mass spectrometry. The two-step dehydrogenation of amine involving a proton coupled electron transfer (PCET) process was revealed for the first time.

Preparation of N,O-Aminals as Synthetic Equivalents of H2C=NAr and (H2C=NHAr)+ ions: Neutral- and Acid-promoted Transformations

A general method for the synthesis of N, O-aminals derived from primary aromatic amines is described.The reactivity of these compounds under neutral and acidic conditions has been studied and the title compounds can be envisaged as general purpose H2C=NAr or (H2C=NAr)+ equivalents.N,O-Aminals have been converted into perhydrotriazines by moderate heating and into bis(4-aminoaryl)methane derivatives or N-benzylarylamines, respectively, when heated in acidid media with pH control.Reduction od N,O-acetals with sodium cyanoborohydride has revealed that the C-O bond is broken exclusively in acidic media.