Z-Lys(Boc)ψCH₂I

Base Information

Chemical Name:Z-Lys(Boc)ψCH₂I
CAS No.:1622094-01-2
Molecular Formula:C₁₉H₂₉IN₂O₄
Molecular Weight:476.355
Hs Code.:

Synonyms:Z-Lys(Boc)ψCH₂I

Suppliers and Price of Z-Lys(Boc)ψCH₂I

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Z-Lys(Boc)ψCH₂I

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Z-Lys(Boc)ψCH₂I

There total 2 articles about Z-Lys(Boc)ψCH₂I 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: 76.0%

: 122477-82-1
tert-butyl-N-[(5S)-5-(benzyloxycarbonylamino)-6-hydroxyhexyl]carbamate

: 1622094-01-2
Z-Lys(Boc)ψCH₂I

Guidance literature:: With 1H-imidazole; iodine; triphenylphosphine; In dichloromethane; for 2h;
DOI:10.1021/jo500911v

Reference yield:

: 2389-60-8
Z-Lys(Boc)-OH

: 1622094-01-2
Z-Lys(Boc)ψCH₂I

Guidance literature:: Multi-step reaction with 3 steps

1: 4-methyl-morpholine / tetrahydrofuran / -15 °C

2: sodium tetrahydroborate

3: triphenylphosphine; iodine / dichloromethane / 0 °C

With 4-methyl-morpholine; sodium tetrahydroborate; iodine; triphenylphosphine; In tetrahydrofuran; dichloromethane;

Reference yield: 83.0%

: 1622094-01-2
Z-Lys(Boc)ψCH₂I

: Z-Lys(Boc)ψCH₃

Guidance literature:: With palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; at 20 ℃; for 24h; under 2534.09 Torr; Reagent/catalyst; chemoselective reaction;
DOI:10.1021/jo500911v