62869-74-3

Basic information

• Product Name: N-4-NITROBENZYL-N-PROPYLAMINE HYDROCHLORIDE, 99
• Synonyms: n-4-nitrobenzyl-n-n-propylamine;N-4-NITROBENZYL-N-PROPYLAMINE HYDROCHLORIDE, 99;4-Nitro-N-propylbenzylamine hydr;N-(n-Propyl)-4-nitrobenzylaminehydrochloride,99%
• CAS NO: 62869-74-3
• Molecular Formula: C₁₀H₁₄N₂O₂
• Molecular Weight: 230.6913
• Mol File: 62869-74-3.mol

Chemical Properties

• Melting Point: 227-230°C
• Boiling Point: 307.1°Cat760mmHg
• Flash Point: 139.5°C
• Appearance: /
• Density: 1.104g/cm³
• Vapor Pressure: 0.000739mmHg at 25°C
• Refractive Index: 1.54
• CAS DataBase Reference: N-4-NITROBENZYL-N-PROPYLAMINE HYDROCHLORIDE, 99(CAS DataBase Reference)
• NIST Chemistry Reference: N-4-NITROBENZYL-N-PROPYLAMINE HYDROCHLORIDE, 99(62869-74-3)
• EPA Substance Registry System: N-4-NITROBENZYL-N-PROPYLAMINE HYDROCHLORIDE, 99(62869-74-3)

Safety Data

• Hazard Codes: Xi:Irritant
• Statements: R36/37/38:Irritating to eyes, respiratory system and skin.
• Safety Statements: S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S37/39:Wear suitable g
• Hazardous Substances Data: 62869-74-3(Hazardous Substances Data)

Usage

Chemical Properties

yellow crystalline powder

InChI:InChI=1/C10H14N2O2/c1-2-7-11-8-9-3-5-10(6-4-9)12(13)14/h3-6,11H,2,7-8H2,1H3

Upstream product

• 107-10-8 propylamine 
• 100-14-1 4-nitrobenzyl chloride 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 2585-24-2 N-n-propyl-4-nitrobenzamide 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 55245-75-5 C₁₁H₁₃ClN₂O₃ 
• 1227783-82-5 3-(4-fluorophenyl)-N-(4-nitrobenzyl)-N-propylpropionamide 
• 619-50-1 4-nitrobenzoic acid methyl ester 

Relevant articles and documents

Room-Temperature Chemoselective Reductive Alkylation of Amines Catalyzed by a Well-Defined Iron(II) Complex Using Hydrogen

A transition-metal frustrated Lewis pair approach has been envisaged to enhance the catalytic activity of tricarbonyl phosphine-free iron complexes in reduction of amines. A new cyclopentadienyl iron(II) tricarbonyl complex has been isolated, fully characterized, and applied in hydrogenation. This phosphine-free iron complex is the first Earth-abundant metal complex that is able to catalyze chemoselective reductive alkylation of various functionalized amines with functionalized aldehydes. Such selectivity and functionality tolerance (alkenes, esters, ketones, acetals, unprotected hydroxyl groups, and phosphines) have been demonstrated also for the first time at room temperature with an Earth-abundant metal complex. This alkylation reaction was also performed without any preliminary condensation and generated only water as a byproduct. The resulting amines provided rapid access to potential building blocks, metal ligands, or drugs. Density functional theory calculations highlighted first that the formation of the 16 electron species, via the activation of the tricarbonyl complex Fe3, was facilitated and, second, that the hydrogen cleavage did not follow the same pathway as bond breaking, usually described with the known cyclopentadienone iron tricarbonyl complexes (Fe1 and Fe4). These calculations highlighted that the new complex Fe3 does not behave as a bifunctional catalyst, in contrast to its former congeners.

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