71182-60-0

Basic information

• Product Name: Benzenamine, 4-methoxy-N-(2-methylpropyl)-
• CAS NO: 71182-60-0
• Molecular Formula: C11H17NO
• Molecular Weight: 179.262
• Mol File: 71182-60-0.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-methoxy-N-(2-methylpropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-methoxy-N-(2-methylpropyl)-(71182-60-0)
• EPA Substance Registry System: Benzenamine, 4-methoxy-N-(2-methylpropyl)-(71182-60-0)

Safety Data

• Hazardous Substances Data: 71182-60-0(Hazardous Substances Data)

Upstream product

• 623-12-1 4-chloromethoxybenzene 
• 78-81-9 isobutylamine 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 350-46-9 4-Fluoronitrobenzene 
• 100-17-4 para-methoxynitrobenzene 
• 78-83-1 2-methyl-propan-1-ol 
• 458-52-6 2-fluoro-4-(methoxy)aniline 
• 18169-40-9 (4-Methoxy-phenyl)-[2-methyl-prop-(Z)-ylidene]-amine 
• 104-94-9 4-methoxy-aniline 
• 696-62-8 para-iodoanisole 
• 590-86-3 isovaleraldehyde 
• 78-84-2 isobutyraldehyde 
• 137-07-5 2-amino-benzenethiol 
• 84110-40-7 Dihydroxy-isobutyl-boran 

Downstream Products

• 1562-94-3 4,4'-azoxy anisole 

Relevant articles and documents

Catalytic Selective Oxidative Coupling of Secondary N-Alkylanilines: An Approach to Azoxyarene

Azoxyarenes are among important scaffolds in organic molecules. Direct oxidative coupling of primary anilines provides a concise fashion to construct them. However, whether these scaffolds can be prepared from secondary N-alkylanilines is not well explored. Here, we present a catalytic selective oxidative coupling of secondary N-alkylaniline to afford azoxyarene with tungsten catalyst under mild conditions. In addition, azoxy can be viewed as a bioisostere of alkene and amide. Several "azoxyarene analogues" of the corresponding bioactive alkenes and amides showed comparable promising anticancer activities.

Improving C=N bond reductions with (Cyclopentadienone)iron complexes: Scope and limitations

Herein, we broaden the application scope of (cyclo-pentadienone)iron complexes 1 in C=N bond reduction. The catalytic scope of pre-catalyst 1b, which is more active than the “Kn?lker complex” (1a) and other members of its family, has been expanded to the catalytic transfer hydrogenation (CTH) of a wider range of aldimines and ketimines, either pre-isolated or generated in situ. The kinetics of 1b-promoted CTH of ketimine S1 were assessed, showing a pseudo-first order profile, with TOF = 6.07 h–1 at 50 % conversion. Moreover, the chiral complex 1c and its analog 1d were employed in the enantioselective reduction of ketimines and reductive amination of ketones, giving fair to good yields and moderate enantioselectivity.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

Compounds of Formula I with activity against HIV, including pharmaceutical compositions and methods for using these compounds in treating human immunodeficiency virus (HIV) infection, are set forth: Formula :(I)