N-(sulfonatooxy)-N-acetyl-4-aminostilbene

Base Information

Chemical Name:N-(sulfonatooxy)-N-acetyl-4-aminostilbene
CAS No.:211029-25-3
Molecular Formula:C₁₆H₁₄NO₅S
Molecular Weight:332.357
Hs Code.:

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 N-(sulfonatooxy)-N-acetyl-4-aminostilbene

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Technology Process of N-(sulfonatooxy)-N-acetyl-4-aminostilbene

There total 1 articles about N-(sulfonatooxy)-N-acetyl-4-aminostilbene 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:

: 843-23-2
N-hydroxy-N-acetyl-4-aminostilbene

: 211029-25-3
N-(sulfonatooxy)-N-acetyl-4-aminostilbene

Guidance literature:: With sulfuric acid; dicyclohexyl-carbodiimide;
DOI:10.1021/jo980500z

Reference yield: 40.0%

: 211029-25-3
N-(sulfonatooxy)-N-acetyl-4-aminostilbene

: 3-azido-N-acetyl-4-aminostilbene

: N-[4-((1R,2R)-2-Azido-1-hydroxy-2-phenyl-ethyl)-phenyl]-acetamide

: N-[4-((1R,2R)-1,2-Diazido-2-phenyl-ethyl)-phenyl]-acetamide

: N-[4-((1R,2S)-1,2-Diazido-2-phenyl-ethyl)-phenyl]-acetamide

Guidance literature:: With sodium azide; In acetonitrile; Further byproducts given; phosphate buffer, pH 7.2;
DOI:10.1021/jo980500z

Reference yield: 12.4%

: 211029-25-3
N-(sulfonatooxy)-N-acetyl-4-aminostilbene

: 3-azido-N-acetyl-4-aminostilbene

: 60239-58-9
N-[4-((1R,2R)-1,2-Dihydroxy-2-phenyl-ethyl)-phenyl]-acetamide

: N-[4-((1R,2R)-2-Azido-1-hydroxy-2-phenyl-ethyl)-phenyl]-acetamide

: N-[4-((1S,2R)-2-Azido-1-hydroxy-2-phenyl-ethyl)-phenyl]-acetamide

: N-[4-((1R,2R)-1,2-Diazido-2-phenyl-ethyl)-phenyl]-acetamide

: N-[4-((1R,2S)-1,2-Diazido-2-phenyl-ethyl)-phenyl]-acetamide

Guidance literature:: With sodium azide; water; In acetonitrile; at 20 ℃; Rate constant; Product distribution; phosphate buffer, pH 7.2, μ 0.5; hydrolysis in the presence and absence of NaN3; formation of electrophilic intermediates; trapping of intermediates by azide ion and H2O; trapping ratio;
DOI:10.1021/jo980500z