1,2-Bis(4-nitrobenzyl)ethane

Base Information

Chemical Name:1,2-Bis(4-nitrobenzyl)ethane
CAS No.:41854-80-2
Molecular Formula:C16H16N2O4
Molecular Weight:300.3092
Hs Code.:
NSC Number:86419
DSSTox Substance ID:DTXSID60962019
Nikkaji Number:J2.327.391H
Wikidata:Q82943596

Synonyms:41854-80-2;NSC86419;SCHEMBL18913824;DTXSID60962019;NSC-86419;1,1'-(Butane-1,4-diyl)bis(4-nitrobenzene)

Suppliers and Price of 1,2-Bis(4-nitrobenzyl)ethane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 7 raw suppliers

Chemical Property of 1,2-Bis(4-nitrobenzyl)ethane

Chemical Property:

Boiling Point:476.7°Cat760mmHg
Flash Point:224.9°C
Density:1.253g/cm³
XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:300.11100700
Heavy Atom Count:22
Complexity:325

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1CCCCC2=CC=C(C=C2)[N+](=O)[O-])[N+](=O)[O-]

Technology Process of 1,2-Bis(4-nitrobenzyl)ethane

There total 3 articles about 1,2-Bis(4-nitrobenzyl)ethane 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: 92.0%

: 1,4-bis(p-nitrophenyl)-1,2,3-butatriene

: 41854-80-2
1,2-Di-p-nitrobenzylethan

Guidance literature:: With hydrogen; palladium on activated charcoal; In acetone;

Reference yield:

: 6933-17-1
(4-nitrobenzylidene)triphenylphosphorane

: 41854-80-2
1,2-Di-p-nitrobenzylethan

Guidance literature:: Multi-step reaction with 2 steps

1: 48 percent / CH₂Cl₂ / 168 h / 0 °C

2: 92 percent / H₂ / 5percent Pd/C / acetone

With hydrogen; palladium on activated charcoal; In dichloromethane; acetone;