N-(2-nitrobenzyl)cyclopentanamine

Base Information

• Chemical Name: N-(2-nitrobenzyl)cyclopentanamine
• CAS No.: 355814-64-1
• Molecular Formula: C₁₂H₁₆N₂O₂
• Molecular Weight: 220.271
• DSSTox Substance ID: DTXSID90355157
• Wikidata: Q82133851
• Mol file: 355814-64-1.mol

Synonyms:N-(2-nitrobenzyl)cyclopentanamine;355814-64-1;N-[(2-nitrophenyl)methyl]cyclopentanamine;CHEMBRDG-BB 5571297;Cambridge id 5571297;Oprea1_008123;Oprea1_612581;DTXSID90355157;STK145957;AKOS000252950;SB79764;N-CYCLOPENTYL-N-(2-NITROBENZYL)AMINE;AB00089761-01

Chemical Property of N-(2-nitrobenzyl)cyclopentanamine

Chemical Property:

• Vapor Pressure: 8.76E-05mmHg at 25°C
• Boiling Point: 340.2°C at 760 mmHg
• Flash Point: 159.5°C
• Density: 1.15g/cm³
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 220.121177757
• Heavy Atom Count: 16
• Complexity: 234

Purity/Quality:

98% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC(C1)NCC2=CC=CC=C2[N+](=O)[O-]

Technology Process of N-(2-nitrobenzyl)cyclopentanamine

There total 3 articles about N-(2-nitrobenzyl)cyclopentanamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

C12H14N2O2 → N-(2-nitrobenzyl)cyclopentylamine (355814-64-1)

Guidance literature:

With sodium tetrahydroborate; In methanol; at 20 ℃; for 1h;

DOI:10.1002/ardp.201600020

Reference yield:

2-nitro-benzaldehyde (552-89-6) → N-(2-nitrobenzyl)cyclopentylamine (355814-64-1)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium sulfate / methanol / 2 h / 20 °C

2: sodium tetrahydroborate / methanol / 1 h / 20 °C

With sodium tetrahydroborate; sodium sulfate; In methanol;

DOI:10.1002/ardp.201600020

Reference yield:

Cyclopentamine (1003-03-8) → N-(2-nitrobenzyl)cyclopentylamine (355814-64-1)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium sulfate / methanol / 2 h / 20 °C

2: sodium tetrahydroborate / methanol / 1 h / 20 °C

With sodium tetrahydroborate; sodium sulfate; In methanol;

DOI:10.1002/ardp.201600020

upstream raw materials:

2-nitro-benzaldehyde

Cyclopentamine