5369-30-2

Basic information

• Product Name: N-(4-(dimethylamino)phenyl)-N-methylnitrous amide
• Synonyms: N-(4-(dimethylamino)phenyl)-N-methylnitrous amide
• CAS NO: 5369-30-2
• Molecular Weight: 179.222
• Mol File: 5369-30-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(4-(dimethylamino)phenyl)-N-methylnitrous amide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-(dimethylamino)phenyl)-N-methylnitrous amide(5369-30-2)
• EPA Substance Registry System: N-(4-(dimethylamino)phenyl)-N-methylnitrous amide(5369-30-2)

Safety Data

• Hazardous Substances Data: 5369-30-2(Hazardous Substances Data)

Upstream product

• 100-22-1 N,N,N',N'-tetramethyl-para-phenylenediamine 
• 64-19-7 acetic acid 
• 5369-34-6 N,N,N'-trimethyl-p-phenylenediamine 

Downstream Products

• 5369-34-6 N,N,N'-trimethyl-p-phenylenediamine 

Relevant articles and documents

Highly selective sp3 C-N bond activation of tertiary anilines modulated by steric and thermodynamic factors

A highly selective sp3 C-N cleavage of tertiary anilines was achieved using the TBN/TEMPO catalyst system. When N,N-diaklylanilines (alkyl, benzyl) were employed, the N-CH3 bond was selectively cleaved via radical C-H activation. Moreover, when the allyl group was installed, totally reverse selectivity was observed. It is worth noting that the solvent effect is also crucial to obtain high reaction efficiency and selectivity.

S-nitrosation of proteins by N-methyl-N-nitrosoanilines

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Nitrones and Oxaziridines. XLII Synthesis of Indol-3-yl Substituted 1-Pyrroline 1-Oxides

The 1-pyrroline 1-oxides (13), (14), (16) and (18) with indol-3-yl substituents attached to the 2- or 4-positions have been synthesized by reductive cyclization of the related γ-nitro ketones.The corresponding 1-pyrrolines (15), (17) and (19) have also be