75077-46-2

Basic information

• Product Name: Benzenamine, 4-nitro-N-2-propynyl-
• CAS NO: 75077-46-2
• Molecular Formula: C9H8N2O2
• Molecular Weight: 176.175
• Mol File: 75077-46-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-nitro-N-2-propynyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-nitro-N-2-propynyl-(75077-46-2)
• EPA Substance Registry System: Benzenamine, 4-nitro-N-2-propynyl-(75077-46-2)

Safety Data

• Hazardous Substances Data: 75077-46-2(Hazardous Substances Data)

Upstream product

• 350-46-9 4-Fluoronitrobenzene 
• 2450-71-7 Propargylamine 
• 100-01-6 4-nitro-aniline 
• 106-96-7 propargyl bromide 

Downstream Products

• 123685-48-3 N-[3,4-Dihydro-6-[[(4-nitrophenyl)-2-propynylamino]methyl]4-oxo-2-quinazolinyl]-2,2-dimethylpropanamide 
• 111493-06-2 (4-Nitro-phenyl)-prop-2-ynyl-carbamic acid ethyl ester 
• 123685-36-9 2-amino-6-[[(4-nitrophenyl)-2-propynylamino]methyl]-4(3H)-quinazolinone 
• 613-50-3 6-nitroquinoline 
• 1616405-30-1 N-methyl-4-nitro-N-((1-tosyl-1H-1,2,3-triazol-4-yl)methyl)aniline 
• 1616405-40-3 (E)-4-methyl-N-((1-methyl-5-nitro-1H-indol-3-yl)methylene)benzenesulfonamide 
• 111493-14-2 5-[1-Iodo-meth-(E)-ylidene]-3-(4-nitro-phenyl)-oxazolidin-2-one 
• 111493-23-3 3-(4-Nitro-phenyl)-5-prop-2-yn-(E)-ylidene-oxazolidin-2-one 
• 100-01-6 4-nitro-aniline 
• 109769-27-9 N-methyl-4-nitro-N-(prop-2-yn-1-yl)aniline 
• 1449498-93-4 N¹-methyl-N¹-(prop-2-yn-1-yl)benzene-1,4-diamine 

Relevant articles and documents

New Hydroxyquinoline-Based Derivatives as Potent Modulators of Amyloid-β Aggregations

Copper and zinc have been found to contribute to the burden of amyloid-β (Aβ) aggregations in neurodegenerative Alzheimer's disease (AD). Dysregulation of these metals leads to the generation of reactive oxygen species (ROS) and eventually results in oxid

Anticancer (hexacarbonyldicobalt)propargyl aryl ethers: Synthesis, antiproliferative activity, apoptosis induction, and effect on cellular oxidative stress

While an increasing number of (hexacarbonyldicobalt)alkynes have been found to possess antiproliferative activity against a number of cancer cell lines, the role of the organometallic moiety in this bioactivity is not well understood. To gain a better und

Intramolecular aromatic substitution and amino-claisen rearrangement in substituted N-(2-propynyl)anilines on electron impact

N-(2-Propynyl)anilines undergo amino-Claisen rearrangement to a minor extent in the ion source, losing a molecule of HCN under electron impact conditions. However, metastable molecular ions with energies closer to threshold undergo Claisen rearrangement g