1-(5-Nitropyridin-2-yl)-1,4-diazepane

Base Information

• Chemical Name: 1-(5-Nitropyridin-2-yl)-1,4-diazepane
• CAS No.: 287114-27-6
• Molecular Formula: C₁₀H₁₄N₄O₂
• Molecular Weight: 222.247
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID60951362
• Wikidata: Q82929646
• Mol file: 287114-27-6.mol

Synonyms:287114-27-6;1-(5-nitropyridin-2-yl)-1,4-diazepane;1-(5-Nitropyridin-2-yl)homopiperazine;1-(5-nitro-2-pyridyl)-1,4-diazepane;MFCD01311911;1H-1,4-Diazepine, hexahydro-1-(5-nitro-2-pyridinyl)-;Maybridge1_000445;Oprea1_353430;SCHEMBL2003294;HMS542M05;DTXSID60951362;1-(5-nitropyrid-2-yl)homopiperazine;AKOS000129499;AS-78420;1-(5-nitro-pyridin-2-yl)-[1,4]diazepane;CS-0316263;FT-0605796

Chemical Property of 1-(5-Nitropyridin-2-yl)-1,4-diazepane

Chemical Property:

• Vapor Pressure: 2.54E-07mmHg at 25°C
• Melting Point: 111 °C
• Refractive Index: 1.567
• Boiling Point: 421.8 °C at 760 mmHg
• Flash Point: 208.9 °C
• PSA: 73.98000
• Density: 1.23 g/cm³
• LogP: 1.70650
• XLogP3: 0.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• Exact Mass: 222.11167570
• Heavy Atom Count: 16
• Complexity: 244

Purity/Quality:

98%min ^*data from raw suppliers

1-(5-Nitropyridin-2-yl)-1,4-diazepane ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 10-34
• Safety Statements: 16-26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CNCCN(C1)C2=NC=C(C=C2)[N+](=O)[O-]

Technology Process of 1-(5-Nitropyridin-2-yl)-1,4-diazepane

There total 1 articles about 1-(5-Nitropyridin-2-yl)-1,4-diazepane 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:

1,4-Diazacycloheptane (505-66-8) + 2-chloro-5-nitropyridine (4548-45-2) → 1-(5-nitro-pyridin-2-yl)homopiperazine (287114-27-6) + 1-(5-carbomethoxy-pyridin-2-yl)homopiperazine

Guidance literature:

In ethyl acetate; toluene;

upstream raw materials:

1,4-Diazacycloheptane

2-chloro-5-nitropyridine

Refernces

• 1、 -. "AMIDE DERIVATIVES AND DRUG COMPOSITIONS". . . Retrieved 2008/06/13.