35666-61-6

Basic information

• Product Name: Benzenamine, 3-methoxy-N,N-dipropyl-
• CAS NO: 35666-61-6
• Molecular Formula: C13H21NO
• Molecular Weight: 207.316
• Mol File: 35666-61-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenamine, 3-methoxy-N,N-dipropyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 3-methoxy-N,N-dipropyl-(35666-61-6)
• EPA Substance Registry System: Benzenamine, 3-methoxy-N,N-dipropyl-(35666-61-6)

Safety Data

• Hazardous Substances Data: 35666-61-6(Hazardous Substances Data)

Upstream product

• 536-90-3 m-Anisidine 
• 107-08-4 1-iodo-propane 
• 513-08-6 phosphoric acid tripropyl ester 
• 107-12-0 propiononitrile 
• 43141-68-0 3-(di-n-propylamino)phenol 
• 80-48-8 methyl p-toluene sulfonate 
• 90-04-0 2-methoxy-phenylamine 
• 106-94-5 propyl bromide 

Downstream Products

• 1032716-19-0 3-Methoxy-4-nitroso-N,N-dipropylaniline 
• 131190-89-1 C₁₄H₂₁NO₂ 

Relevant articles and documents

Syntheses and photophysical properties of aminobenzopyranoxanthene dyes containing various alkyl chains at amine moieties

Aminobenzopyranoxanthene (ABPX) dyes containing linear n-alkyl chains at amino groups were synthesized, and their cis and trans stereoisomers were isolated. Detailed spectrophotometric studies revealed that all the ABPX derivatives exhibited fluorescence emission in the far-red and near-infrared wavelength regions, and their fluorescence quantum efficiency increased with increasing n-alkyl chain length. Almost no differences in photophysical properties were observed between the cis and trans stereoisomers.

Synthesis and in vitro antiprotozoal activities of water-soluble, inexpensive 3,7-bis(dialkylamino)phenoxazin-5-ium derivatives

3,7-Bis(dialkylamino)phenoxazinium salts were synthesized and evaluated for in vitro activities against Plasmodium falciparum, Trypanosoma cruzi, T. brucei rhodesiense, and Leishmania donovani. Notably, the compounds showed potent antiprotozoal activities, especially against P. falciparum and T. cruzi. The compounds with alkyl side chains less than three carbons in length possessed good activities with high selective indices.

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.