L-phenylalanyllaurylamide hydrochloride

Base Information

Chemical Name:L-phenylalanyllaurylamide hydrochloride
CAS No.:73048-85-8
Molecular Formula:C₂₁H₃₆N₂O*ClH
Molecular Weight:368.991
Hs Code.:

Synonyms:L-phenylalanyllaurylamide hydrochloride

Suppliers and Price of L-phenylalanyllaurylamide hydrochloride

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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 L-phenylalanyllaurylamide hydrochloride

Chemical Property:

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Technology Process of L-phenylalanyllaurylamide hydrochloride

There total 4 articles about L-phenylalanyllaurylamide hydrochloride 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: 97.0%

: Boc-Phe-NH-(CH₂)11-CH₃

: 73048-85-8
L-phenylalanyllaurylamide hydrochloride

Guidance literature:: With hydrogenchloride; In ethyl acetate; at 20 ℃;
DOI:10.1002/pep2.24155

Reference yield:

: 124-22-1
n-Dodecylamine

: 73048-85-8
L-phenylalanyllaurylamide hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: benzotriazol-1-ol; dicyclohexyl-carbodiimide / N,N-dimethyl-formamide / -5 - 20 °C

2: hydrogenchloride / ethyl acetate / 20 °C

With hydrogenchloride; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.12.051

Reference yield:

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 73048-85-8
L-phenylalanyllaurylamide hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: benzotriazol-1-ol; dicyclohexyl-carbodiimide / N,N-dimethyl-formamide / -5 - 20 °C

2: hydrogenchloride / ethyl acetate / 20 °C

With hydrogenchloride; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.12.051