C₃₅H₄₃NO₄

Base Information

Chemical Name:C₃₅H₄₃NO₄
CAS No.:1426257-76-2
Molecular Formula:C₃₅H₄₃NO₄
Molecular Weight:541.731
Hs Code.:

C<sub>35</sub>H<sub>43</sub>NO<sub>4</sub>

Synonyms:C₃₅H₄₃NO₄

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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 C₃₅H₄₃NO₄

Chemical Property:

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Technology Process of C₃₅H₄₃NO₄

There total 3 articles about C₃₅H₄₃NO₄ 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: 89.0%

: 68-22-4
norethisterone

: 1426257-64-8
C₁₅H₁₇NO₂

: 1426257-76-2
C₃₅H₄₃NO₄

Guidance literature:: With Wilkinson's catalyst; In chloroform; at 50 ℃; for 24h; regioselective reaction; Inert atmosphere;
DOI:10.1039/c3cc40634b

Reference yield:

: 4755-50-4
4-(dimethylamino)benzoyl chloride

: 1426257-76-2
C₃₅H₄₃NO₄

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran / 0.33 h / -78 - 20 °C / Inert atmosphere

1.2: 20 °C / Inert atmosphere

2.1: Wilkinson's catalyst / chloroform / 24 h / 50 °C / Inert atmosphere

With Wilkinson's catalyst; n-butyllithium; In tetrahydrofuran; chloroform;
DOI:10.1039/c3cc40634b

Reference yield:

: 619-84-1
p-N,N-dimethylaminobenzoic acid

: 1426257-76-2
C₃₅H₄₃NO₄

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride / toluene / 6 h / Reflux; Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran / 0.33 h / -78 - 20 °C / Inert atmosphere

2.2: 20 °C / Inert atmosphere

3.1: Wilkinson's catalyst / chloroform / 24 h / 50 °C / Inert atmosphere

With Wilkinson's catalyst; n-butyllithium; thionyl chloride; In tetrahydrofuran; chloroform; toluene;
DOI:10.1039/c3cc40634b