17408-47-8

Basic information

• Product Name: Benzoyl(2-methylpyridinium-1-yl)amine anion
• Synonyms: Benzoyl(2-methylpyridinio)amine anion;Benzoyl(2-methylpyridinium-1-yl)amine anion;hydroxide inner salt
• CAS NO: 17408-47-8
• Molecular Formula: C₁₃H₁₂N₂O
• Molecular Weight: 0
• Mol File: 17408-47-8.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzoyl(2-methylpyridinium-1-yl)amine anion(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl(2-methylpyridinium-1-yl)amine anion(17408-47-8)
• EPA Substance Registry System: Benzoyl(2-methylpyridinium-1-yl)amine anion(17408-47-8)

Safety Data

• Hazardous Substances Data: 17408-47-8(Hazardous Substances Data)

Upstream product

• 109-06-8 α-picoline 
• 56150-02-8 1-amino-2-methyl-pyridinium 2,4-dinitro-phenolate 
• 98-88-4 benzoyl chloride 
• 51135-75-2 2-methylpyridine N-imine 

Downstream Products

• 1020416-45-8 C₁₉H₁₆N₂O 
• 1619940-77-0 C₁₉H₁₆N₂O 
• 1429338-01-1 benzoyl(2-methyl-6-neopentylpyridinium-1-yl)azanide 
• 1337985-07-5 2-phenylpyrazolo[1,5-a]pyridin-3-yl acetate 
• 51118-88-8 2-phenylpyrazolo[1,5-a]pyridin-3-yl benzoate 
• 1103509-71-2 N-(2-methyl-3,6-dihydro-2H-pyridin-1-yl)-benzamide 
• 1020416-44-7 (2-benzhydrylpyridinium-1-yl)(benzoyl)azanide 
• 1020416-32-3 C₂₆H₂₀N₂O₂ 
• 1020416-35-6 C₂₀H₁₅F₃N₂O 
• 1020416-34-5 C₂₄H₂₅N₃O₃ 
• 1020416-33-4 C₁₉H₁₅FN₂O 
• 1020416-26-5 C₂₀H₁₈N₂O 
• 1020416-28-7 C₂₀H₁₈N₂O 
• 1020416-27-6 C₂₀H₁₈N₂O 

Relevant articles and documents

Benzoyl peroxide promoted radical ortho-alkylation of nitrogen heteroaromatics with simple alkanes and alcohols

A catalytic amount of benzoyl peroxide (BPO)-initiated cross-dehydrogenative coupling reaction of N-iminopyridine ylides with simple alkanes and alcohols leads to the corresponding 2-alkylpyridines with high regioselectivity in moderate to good yields without an additional reduction step to remove the activated group. A catalytic amount of benzoyl peroxide (BPO)-initiated cross-dehydrogenative coupling reaction of N-iminopyridine ylides with simple alkanes and alcohols has been developed. The strategy allowed convenient access to various 2-alkylpyridines in moderate to good yields without an additional reduction step to remove the activated group.

Catalytic asymmetric hydrogenation of N-iminopyridinium ylides: Expedient approach to enantioenriched substituted piperidine derivatives

We have developed an efficient catalytic enantioselective hydrogenation of pyridine derivatives. Enhanced reactivity was possible by an optimization of the electronic properties of the catalyst through ligand modification. This methodology shows the parti

Complexation promoted additions to N-benzoyliminopyridinium ylides. A novel and highly regioselective approach to polysubstituted piperidines

Unprecedented regioselectivities were observed for the addition of different organometallic nucleophiles to N-benzoyliminopyridinium ylides. Even benzylic and branched aliphatic Grignard reagents, which usually give substantial amounts of 1,4-adducts, sho