β-(p-Nitrophenyl)isoserin

Base Information

Chemical Name:β-(p-Nitrophenyl)isoserin
CAS No.:55610-84-9
Molecular Formula:C₉H₁₀N₂O₅
Molecular Weight:226.189
Hs Code.:

Synonyms:

Suppliers and Price of β-(p-Nitrophenyl)isoserin

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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 β-(p-Nitrophenyl)isoserin

Chemical Property:

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Technology Process of β-(p-Nitrophenyl)isoserin

There total 3 articles about β-(p-Nitrophenyl)isoserin 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:

: 882-06-4
4-nitro-trans-cinnamic acid

: 10098-38-1
p-nitrophenylserine

: 55610-84-9
β-(p-Nitrophenyl)isoserin

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogencarbonate; oxone; edetate disodium / acetone; water / 7 h / 25 °C / pH 7.5

1.2: pH 2

2.1: potassium hydroxide / ethanol / Cooling with ice

3.1: (S)-2-amino-5-phenylpent-4-enoic acid / aq. phosphate buffer / pH 8 / Enzymatic reaction

With oxone; edetate disodium; sodium hydrogencarbonate; (S)-2-amino-5-phenylpent-4-enoic acid; potassium hydroxide; In aq. phosphate buffer; ethanol; water; acetone;
DOI:10.1021/acscatal.9b01557

Reference yield:

: 56010-46-9
3-(4-nitro-phenyl)-oxiranecarboxylic acid

: 10098-38-1
p-nitrophenylserine

: 55610-84-9
β-(p-Nitrophenyl)isoserin

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / ethanol / Cooling with ice

2: (S)-2-amino-5-phenylpent-4-enoic acid / aq. phosphate buffer / pH 8 / Enzymatic reaction

With (S)-2-amino-5-phenylpent-4-enoic acid; potassium hydroxide; In aq. phosphate buffer; ethanol;
DOI:10.1021/acscatal.9b01557