107411-43-8

Basic information

• Product Name: Benzenamine, 4-methoxy-N,N-dipropyl-
• CAS NO: 107411-43-8
• Molecular Formula: C13H21NO
• Molecular Weight: 207.316
• Mol File: 107411-43-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-methoxy-N,N-dipropyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-methoxy-N,N-dipropyl-(107411-43-8)
• EPA Substance Registry System: Benzenamine, 4-methoxy-N,N-dipropyl-(107411-43-8)

Safety Data

• Hazardous Substances Data: 107411-43-8(Hazardous Substances Data)

Upstream product

• 4346-59-2 para-methoxyphenyldiazonium chloride 
• 142-84-7 di-n-propylamine 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 100-17-4 para-methoxynitrobenzene 
• 107-12-0 propiononitrile 

Relevant articles and documents

Synthesis of a sensitive and selective potassium-sensing fluoroionophore

"Chemical Equation Presented" An efficient synthesis is reported that delivers in 5 steps and 52% overall yield a new structurally simplified fluorescent K+ sensor with improved K+ sensitivity and selectivity over existing K+ sensors. The synthesis procedure utilizes a new template-directed oxidative C-N bond-forming macrocyclization reaction and reports new approaches to Pd(O), Sandmeyer-like and metal-free aminoarylations, as well as organotitanium additions to vinylogous sulfonates.

Reductive monoalkylation of aromatic and aliphatic nitro compounds and the corresponding amines with nitriles

(Chemical Equation Presented) A simple, selective, rapid, and efficient procedure for the synthesis of secondary amines from the reductive alkylation of either aliphatic or aromatic nitro compounds and the corresponding amines is reported. Ammonium formate is used as the hydrogen source and Pd/C as the hydrogen transfer catalyst. The reaction is carried out at room temperature. The rate differences for the preferential formation of secondary over tertiary products are due to both steric and electronic factors.