N-tBOC-L-tryptophan 4-hydroxyphenacyl ester

Base Information

Chemical Name:N-tBOC-L-tryptophan 4-hydroxyphenacyl ester
CAS No.:1365571-06-7
Molecular Formula:C₂₄H₂₆N₂O₆
Molecular Weight:438.48
Hs Code.:

Synonyms:N-tBOC-L-tryptophan 4-hydroxyphenacyl ester

Suppliers and Price of N-tBOC-L-tryptophan 4-hydroxyphenacyl ester

Supply Marketing:

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

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of N-tBOC-L-tryptophan 4-hydroxyphenacyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Technology Process of N-tBOC-L-tryptophan 4-hydroxyphenacyl ester

There total 1 articles about N-tBOC-L-tryptophan 4-hydroxyphenacyl ester 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: 98.0%

: 2491-38-5
2-bromo-1-(4'-hydroxyphenyl)-1-ethanone

: 13139-14-5
Boc-Trp-OH

: 1365571-06-7
N-tBOC-L-tryptophan 4-hydroxyphenacyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2012.02.097

Reference yield:

: 1365571-06-7
N-tBOC-L-tryptophan 4-hydroxyphenacyl ester

: 1365571-07-8
C₂₄H₂₆N₂O₈

Guidance literature:: With ozone; In methanol; at -20 - -15 ℃;
DOI:10.1016/j.bmcl.2012.02.097

Reference yield:

: 1365571-06-7
N-tBOC-L-tryptophan 4-hydroxyphenacyl ester

: L-kynurenine 4-hydroxyphenacyl ester dihydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: ozone / methanol / -20 - -15 °C

2: trifluoroacetic acid / dichloromethane; water

With ozone; trifluoroacetic acid; In methanol; dichloromethane; water;
DOI:10.1016/j.bmcl.2012.02.097