1613-90-7

Basic information

• Product Name: Benzenamine, 4-methoxy-N-(phenylmethylene)-, (E)-
• CAS NO: 1613-90-7
• Molecular Formula: C14H13NO
• Molecular Weight: 211.263
• Mol File: 1613-90-7.mol
• Article Data: 67

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-methoxy-N-(phenylmethylene)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-methoxy-N-(phenylmethylene)-, (E)-(1613-90-7)
• EPA Substance Registry System: Benzenamine, 4-methoxy-N-(phenylmethylene)-, (E)-(1613-90-7)

Safety Data

• Hazardous Substances Data: 1613-90-7(Hazardous Substances Data)

Upstream product

• 116027-51-1 N,N-bis-(4-methoxyphenyl)-1,2-diphenylethane-1,2-diamine 
• 618-31-5 benzylidene dibromide 
• 104-94-9 4-methoxy-aniline 
• 1696-17-9 N,N-diethylbenzamide 
• 2101-87-3 p-methoxy-phenylazide 
• 100-52-7 benzaldehyde 
• 100-17-4 para-methoxynitrobenzene 
• 100-46-9 benzylamine 
• 100-42-5 styrene 
• 1018069-38-9 (E)-2-bromo-4-styrylphenol 
• 3391-75-1 2-methoxy-4-((E)-phenylethenyl)phenol 
• 6554-98-9 trans-4-Hydroxystilbene 
• 18493-15-7 2-[(E/Z)-2-phenylvinyl]phenol 
• 785-81-9 4-nitro-N-(phenylmethylene)benzenamine 

Downstream Products

• 802-49-3 3-(4-methoxyphenylamino)-1,3-diphenyl-1-propanone 
• 150562-30-4 4-methoxy-N-(1-phenylbut-3-enyl)aniline 
• 787617-84-9 (-)-(3R,4S,7R)-5-benzyloxycarbonyl-7-(tert-butyldimethylsilyloxy)-2-(4-methoxyphenyl)-3-phenyl-2,5-diazaspiro[3.4]octan-1-one 
• 787617-86-1 (+)-(3S,4R,7R)-5-benzyloxycarbonyl-7-(tert-butyldimethylsilyloxy)-2-(4-methoxyphenyl)-3-phenyl-2,5-diazaspiro[3.4]octan-1-one 
• 95166-86-2 4-Brom-β-p-anisidino-β-phenyl-propiophenon 
• 95005-67-7 4-Chlor-β-p-anisidino-β-phenyl-propiophenon 
• 5855-65-2 2,4-diphenyl-6-methoxyquinoline 

Relevant articles and documents

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Photoredox-Catalyzed Four-Component Reaction for the Synthesis of Complex Secondary Amines

The one-pot sulfonylation/aminoalkylation of styrene derivatives furnishing substituted ?3-sulfonylamines was accomplished through a photoredox-catalyzed four-component reaction. Besides one molecule of water and the sodium counterion of the sulfinate, all atoms of the starting materials are transferred to the final product, rendering this process highly atom-efficient. The operationally simple protocol allows for the simultaneous formation of three new single bonds (C-S, C-N, and C-C) and therefore grants rapid access to structurally diverse products.