C₃₅H₃₇N₃O₅

Base Information

Chemical Name:C₃₅H₃₇N₃O₅
CAS No.:1448302-56-4
Molecular Formula:C₃₅H₃₇N₃O₅
Molecular Weight:579.696
Hs Code.:

C<sub>35</sub>H<sub>37</sub>N<sub>3</sub>O<sub>5</sub>

Synonyms:

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

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Chemical Property of C₃₅H₃₇N₃O₅

Chemical Property:

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Technology Process of C₃₅H₃₇N₃O₅

There total 5 articles about C₃₅H₃₇N₃O₅ 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:

: 824-94-2
p-methoxybenzyl chloride

: 1448302-56-4
C₃₅H₃₇N₃O₅

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate / N,N-dimethyl-formamide / 20 °C

2: toluene-4-sulfonic acid / ethyl acetate; ethanol / 2 h / 0 - 20 °C

3: triethylamine / dichloromethane / 3 h / 4 - 20 °C

4: sodium tris(acetoxy)borohydride; acetic acid / 16 h / 20 °C

With sodium tris(acetoxy)borohydride; caesium carbonate; toluene-4-sulfonic acid; acetic acid; triethylamine; In ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm400823w

Reference yield:

: 71989-26-9
Fmoc-Lys(tert-butoxycarbonyl)

: 1448302-56-4
C₃₅H₃₇N₃O₅

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate / N,N-dimethyl-formamide / 20 °C

2: toluene-4-sulfonic acid / ethyl acetate; ethanol / 2 h / 0 - 20 °C

3: triethylamine / dichloromethane / 3 h / 4 - 20 °C

4: sodium tris(acetoxy)borohydride; acetic acid / 16 h / 20 °C

With sodium tris(acetoxy)borohydride; caesium carbonate; toluene-4-sulfonic acid; acetic acid; triethylamine; In ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm400823w