N-Allyl-4-nitrobenzenemethanamine

Base Information

Chemical Name:N-Allyl-4-nitrobenzenemethanamine
CAS No.:104245-84-3
Molecular Formula:C₁₀H₁₂N₂O₂
Molecular Weight:192.217
Hs Code.:
DSSTox Substance ID:DTXSID901270980
Nikkaji Number:J1.397.113G

Synonyms:SCHEMBL22749543;N-Allyl-4-nitrobenzenemethanamine;DTXSID901270980;AKOS000247552;4-Nitro-N-2-propen-1-ylbenzenemethanamine;104245-84-3

Suppliers and Price of N-Allyl-4-nitrobenzenemethanamine

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-Allyl-4-nitrobenzenemethanamine

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:192.089877630
Heavy Atom Count:14
Complexity:193

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:

Useful:

Canonical SMILES:C=CCNCC1=CC=C(C=C1)[N+](=O)[O-]

Technology Process of N-Allyl-4-nitrobenzenemethanamine

There total 7 articles about N-Allyl-4-nitrobenzenemethanamine 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: 86.0%

: 555-16-8
4-nitrobenzaldehdye

: 107-11-9,30551-89-4
1-amino-2-propene

: 104245-84-3
N-(4-nitrobenzyl)prop-2-en-1-amine

Guidance literature:: With sodium tris(acetoxy)borohydride; In 1,2-dichloro-ethane; at 20 ℃; for 1.5h; Inert atmosphere;
DOI:10.1002/anie.201500636

Reference yield: 78.0%

: 27895-84-7
4-nitrobenzaldehyde N-allylimine

: 104245-84-3
N-(4-nitrobenzyl)prop-2-en-1-amine

Guidance literature:: 4-nitrobenzaldehyde N-allylimine; With C₂₁H₃₉NPPd^(1-)*C₂F₃O₂^(1-); phenylsilane; In chloroform-d1; at 40 ℃; for 44h; Glovebox; Sealed tube;

With water; In chloroform-d1; regioselective reaction; Sealed tube; Glovebox;
DOI:10.1039/c5cy01859e