85176-37-0

Basic information

• Product Name: BenzeneethanaMine, N-Methyl-4-nitro-
• Synonyms: BenzeneethanaMine, N-Methyl-4-nitro-;N-Methyl-4-nitrophenethylaMine
• CAS NO: 85176-37-0
• Molecular Formula: C₉H₁₂N₂O₂
• Molecular Weight: 180.20378
• Mol File: 85176-37-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 125-129 °C(Press: 1 Torr)
• Appearance: /
• Density: 1.130±0.06 g/cm3(Predicted)
• PKA: 9.98±0.10(Predicted)
• CAS DataBase Reference: BenzeneethanaMine, N-Methyl-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: BenzeneethanaMine, N-Methyl-4-nitro-(85176-37-0)
• EPA Substance Registry System: BenzeneethanaMine, N-Methyl-4-nitro-(85176-37-0)

Safety Data

• Hazardous Substances Data: 85176-37-0(Hazardous Substances Data)

Usage

General Description

Benzeneethanamine, N-Methyl-4-nitro-, also known as 4-Nitro-N-methylethylbenzenamine, is an organic compound characterized by a benzenoid aromatic ring and an amine group. It is yellow to brown in color and possesses a semi-solid form. Its predominant use is as a synthetic intermediate in the production of other compounds. Due to its highly reactive nature, the compound can undergo various reactions, providing versatility in its applications in chemical synthesis. However, it should be handled with care due to its potentially harmful or hazardous nature.

Upstream product

• 124562-85-2 N-methyl-N-(2-(4-nitrophenyl)ethyl)trifluoroacetamide 
• 7697-37-2 nitric acid 
• 589-08-2 N-Methyl-N-phenethylamine 
• 25566-63-6 methyl-phenethyl-amine; picrate 
• 24954-63-0 2,2,2-Trifluoro-N-(2-(4-nitrophenyl)ethyl)acetamide 
• 67000-01-5 methyltertbutyl ether 
• 29968-78-3 2-(4-nitrophenyl)ethylamine monohydrochloride 
• 407-25-0 trifluoroacetic anhydride 
• 74-88-4 methyl iodide 
• 98245-61-5 N-methyl-2-(4-nitrophenyl)acetamide 
• 5339-26-4 (4-nitrophenyl)ethyl bromide 
• 74-89-5 methylamine 

Downstream Products

• 125174-47-2 Methyl-[3-(4-nitro-phenoxy)-propyl]-[2-(4-nitro-phenyl)-ethyl]-amine 
• 142752-11-2 1-(4-nitrophenyl)-4-(N-methyl-N-(2-(4-nitrophenyl)ethyl)amino)piperidine 
• 85176-52-9 1-[7,8-Dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-methyl-N-(2-{4-nitro-phenyl}-ethyl)-amino]-propane hydrochloride 
• 282541-70-2 methyl-[2-(4-nitro-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 6406-74-2 4-(dimethylaminomethyl)aniline 
• 1207199-66-3 C₄₁H₆₈N₄O₁₃ 
• 115256-47-8 methyl-bis-(4-nitro-phenethyl)-amine 
• 115256-44-5 1-(4-methanesulphonamidophenoxy)-2-[N-methyl-N-(4-nitrophenethyl)amino]ethane 
• 119198-12-8 N-Methyl-N-(5-nitrobenzofur-2-ylmethyl)-4-nitrophenethylamine 
• 125174-76-7 N-[2-(2-{[2-(4-Methanesulfonylamino-phenyl)-ethyl]-methyl-amino}-ethoxy)-phenyl]-methanesulfonamide 

Relevant articles and documents

Iron-Catalyzed Intramolecular C—H Amidation of N-Benzoyloxyureas

A redox-neutral Fe-catalyzed intramolecular C—H amidation of N-benzoyloxyureas is described. This methodology employs a simple iron complex in situ generated from Fe(OTf)2 and bipyridine as the catalyst and N-benzoyloxyureas as the nitrene prec

METHODS OF USING SEMI-SYNTHETIC GLYCOPEPTIDES AS ANTIBACTERIAL AGENTS

Methods of using semi-synthetic glycopeptides of formula I-XIV having antibacterial activity are described.

(Phenylalkylaminoalkyloxy)-heteroaryl-compounds, processes and intermediates for their production and pharmaceutical compositions containing them

3-(Phenylalkylaminoalkylozy)-heteroaryl compounds having heart rate lowering and/or anti-ischemic effects, methods for their preparation and pharmaceutical compositions containing them are described. The compounds correspond to the general formula I STR1 or to the general formula XXXI STR2 in which the substituents have the meanings given the specification.