Boc-Lys(2-Cl-Z)-OH|CS-W011662|54613-99-9

Boc-Lys(2-Cl-Z)-OH

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Sku TS246CS-W011662_10_G
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Product Information

Product Name
Boc-Lys(2-Cl-Z)-OH
Brand Name
ChemScene
Product Number
CS-W011662
CAS
54613-99-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7269331
IUPAC Name
(2S)-6-(2-chlorophenyl)methoxycarbonylamino-2-(2-methylpropan-2-yl)oxycarbonylaminohexanoic acid
InChI Key
ATUMDPHEFWGCJF-HNNXBMFYSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CCCCNC(=O)OCC1=CC=CC=C1Cl)C(=O)O

References

In Situ Neutralization Protocols for Boc-SPPS
Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2020
DOI: 10.1007/978-1-0716-0227-0_3

Semisynthesis of Membrane-Attached Proteins Using Split Inteins
Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2017
DOI: 10.1007/978-1-4939-6451-2_7

Synthesis and SAR Studies of Bisthiourea Derivatives of Dipeptides Lys/lys-Asp, Lys/lys-Trp Conjugated Benzo[d]isoxazole as Promising Antioxidants
Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2016-09-29
DOI: 10.1007/s10989-016-9557-1

Quantification of plasma HIV RNA using chemically engineered peptide nucleic acids
Publication Name: Nature Communications
Publication Date: 2014-10-06
DOI: 10.1038/ncomms6079

Design, Synthesis, and Study of Fluorinated Proteins
Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2014
DOI: 10.1007/978-1-4939-1486-9_5