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C28H30N2O4

Base Information Edit
C<sub>28</sub>H<sub>30</sub>N<sub>2</sub>O<sub>4</sub>

Synonyms:C28H30N2O4

Suppliers and Price of C28H30N2O4
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C28H30N2O4 Edit
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Technology Process of C28H30N2O4

There total 1 articles about C28H30N2O4 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:
Guidance literature:
With tribromoacetic acid; C19H24N2O; In toluene; at -40 - 23 ℃; optical yield given as %ee; enantioselective reaction;
DOI:10.1038/nature10232
Guidance literature:
C28H30N2O4; With Wilkinson's catalyst; benzonitrile; In toluene; at 120 ℃;
phosgene; With triethylamine; In toluene; at -45 - 23 ℃;
(Z)-4-bromo-3-iodobut-2-en-1-yl acetate; Further stages;
DOI:10.1038/nature10232
Guidance literature:
Multi-step reaction with 4 steps
1.1: Wilkinson's catalyst; benzonitrile / toluene / 120 °C
1.2: -45 - 23 °C
2.1: tetrabutyl-ammonium chloride; palladium diacetate; sodium hydrogencarbonate / ethyl acetate / 23 °C
3.1: thiophenol; trifluoroacetic acid / 45 °C
4.1: sodium acetate; acetic anhydride / acetic acid / 120 °C
With Wilkinson's catalyst; tetrabutyl-ammonium chloride; sodium acetate; palladium diacetate; acetic anhydride; sodium hydrogencarbonate; thiophenol; benzonitrile; trifluoroacetic acid; In acetic acid; ethyl acetate; toluene; 2.1: Heck reaction;
DOI:10.1038/nature10232
upstream raw materials:

Propargylic aldehyde

Downstream raw materials:

C27H30N2O3

strychnidin-10-one

C24H26N2O3

C27H31IN2O3

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