30438-96-1

Basic information

• Product Name: N,N-diallyl-3-nitroaniline
• Synonyms: N,N-diallyl-3-nitroaniline
• CAS NO: 30438-96-1
• Molecular Weight: 218.255
• Mol File: 30438-96-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N,N-diallyl-3-nitroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-diallyl-3-nitroaniline(30438-96-1)
• EPA Substance Registry System: N,N-diallyl-3-nitroaniline(30438-96-1)

Safety Data

• Hazardous Substances Data: 30438-96-1(Hazardous Substances Data)

Upstream product

• 107-18-6 allyl alcohol 
• 99-09-2 3-nitro-aniline 
• 106-95-6 allyl bromide 
• 4873-09-0 allyl tosylate 

Downstream Products

• 944149-25-1 N,N-diallyl-m-phenylenediamine 
• 69962-41-0 N-(3-(diallylamino)phenyl)acetamide 
• 4310-42-3 1-(3-nitrophenyl)-1H-pyrazole 
• 944149-95-5 C₂₅H₃₂N₆O₂ 
• 944149-93-3 C₁₇H₁₃ClN₂O₂ 
• 944149-83-1 ((HOOCCH₂)2NCH₂CH₂N(CH₂COOH)CH₂CH₂N(CH₂COOH)CH₂CONHNC₉H₅OC₆H₅) 
• 944149-82-0 C₂₁H₂₀N₂O 
• 944149-74-0 ((HOOCCH₂)2NCH₂CH₂N(CH₂COOH)CH₂CH₂N(CH₂COOH)CH₂CONHNC₉H₅OC₂HN₃CH₂C₆H₅) 
• 944149-73-9 C₁₈H₁₅N₅O 
• 944149-68-2 ((HOOCCH₂)2NCH₂CH₂N(CH₂COOH)CH₂CH₂N(CH₂COOH)CH₂CONHNC₉H₅OC₆H₄CH₃) 
• 944149-67-1 C₁₆H₁₄N₂O 
• 944149-66-0 C₂₂H₂₂N₂O 
• 944149-65-9 ((HOOCCH₂)2NCH₂CH₂N(CH₂COOH)CH₂CH₂N(CH₂COOH)CH₂CONHNC₉H₅OC₆H₄OCH₃) 
• 944149-64-8 C₁₆H₁₄N₂O₂ 

Relevant articles and documents

Intermolecular energy transfer from Tb3+ to Eu3+ in aqueous aggregates and on the surface of human cells

Efficient intermolecular energy transfer from carbostyril 124-sensitized Tb3+ to Eu3+ in aqueous aggregates is reported. This energy transfer was also recapitulated on the cell surface of a human kidney cell line (HEK-293T) and imaged by fluorescence microscopy as an example for the applicability of this energy transfer probe for imaging in biological systems.

Palladium-catalyzed allylation of acidic and less nucleophilic anilines using allylic alcohols directly

The direct activation of C-O bonds in allylic alcohols by palladium complexes has been accelerated by carrying out the reactions in the presence of titanium(IV) isoproxide and 4 A molecular sieves. The acidic and less nucleophilic anilines such as diphenylamine, phenothiazine, 4-cyanoaniline, and nitroanilines are efficiently allylated under palladium catalysis using allylic alcohols as allylating reagents.