(S)-2-N-(benzyloxycarbonyl)serinol monovalerate

Base Information

Chemical Name:(S)-2-N-(benzyloxycarbonyl)serinol monovalerate
CAS No.:114838-35-6
Molecular Formula:C₁₆H₂₃NO₅
Molecular Weight:309.362
Hs Code.:

Synonyms:(S)-2-N-(benzyloxycarbonyl)serinol monovalerate

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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 (S)-2-N-(benzyloxycarbonyl)serinol monovalerate

Chemical Property:

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Technology Process of (S)-2-N-(benzyloxycarbonyl)serinol monovalerate

There total 4 articles about (S)-2-N-(benzyloxycarbonyl)serinol monovalerate 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: 55.0%

: 114838-36-7
2-N-(benzyloxycarbonyl)serinol divalerate

: 114838-35-6
(S)-2-N-(benzyloxycarbonyl)serinol monovalerate

Guidance literature:: In water; porcine pancreatic lipase catalyzed hydrolysis;
DOI:10.1021/jo00248a046

Reference yield:

: 5873-43-8
vinyl valerate

: 114838-35-6
(S)-2-N-(benzyloxycarbonyl)serinol monovalerate

Guidance literature:: Multi-step reaction with 2 steps

1: 75 mg / porcine pancreas / tetrahydrofuran / 11 h / 28 °C

2: 55 percent / phosphate buffer, pH 7 / porcine pancreas

With phosphate buffer; porcine pancreas; In tetrahydrofuran;
DOI:10.1021/ja00229a041

Reference yield:

: 71811-26-2
N-Benzyloxycarbonyl-1,3-dihydroxy-2-aminopropane

: 114838-35-6
(S)-2-N-(benzyloxycarbonyl)serinol monovalerate

Guidance literature:: Multi-step reaction with 2 steps

1: 75 mg / porcine pancreas / tetrahydrofuran / 11 h / 28 °C

2: 55 percent / phosphate buffer, pH 7 / porcine pancreas

With phosphate buffer; porcine pancreas; In tetrahydrofuran;
DOI:10.1021/ja00229a041