2-nitrobenzyl penta-2,3-dienoate

Base Information

Chemical Name:2-nitrobenzyl penta-2,3-dienoate
CAS No.:1262883-59-9
Molecular Formula:C₁₂H₁₁NO₄
Molecular Weight:233.224
Hs Code.:

Synonyms:2-nitrobenzyl penta-2,3-dienoate

Suppliers and Price of 2-nitrobenzyl penta-2,3-dienoate

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 0 raw suppliers

Chemical Property of 2-nitrobenzyl penta-2,3-dienoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-nitrobenzyl penta-2,3-dienoate

There total 2 articles about 2-nitrobenzyl penta-2,3-dienoate 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:

: 612-25-9
2-Nitrobenzyl alcohol

: 1262883-59-9
2-nitrobenzyl penta-2,3-dienoate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 0 - 20 °C

2: sodium hydroxide / dichloromethane

3: triethylamine

With triethylamine; sodium hydroxide; In dichloromethane;
DOI:10.1021/acs.orglett.6b00981

Reference yield:

: Br^(1-)*C₂₇H₂₃NO₄P⁽¹⁺⁾

: 79-03-8
propionyl chloride

: 1262883-59-9
2-nitrobenzyl penta-2,3-dienoate

Guidance literature:: With triethylamine;
DOI:10.1039/c0cc02270e

Reference yield: 33.0%

: 1262977-13-8,1303527-12-9,1175712-33-0,1177425-14-7
pinacolato bis(2-hydroxypropyl)aminodiboron

: 1262883-59-9
2-nitrobenzyl penta-2,3-dienoate

: 1262884-12-7
(Z)-2-nitrobenzyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pent-3-enoate

Guidance literature:: With 2,2,2-trifluoroethanol; copper(l) chloride; In tetrahydrofuran; at 20 ℃; stereoselective reaction; Inert atmosphere;
DOI:10.1039/c0cc02270e