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Boc-S-benzyl-L-cysteine, 99%|120799|5068-28-0

Boc-S-benzyl-L-cysteine, 99%

Cat. No JKB10022_25_G
J&K Chemical

Product Information

Product Name
Boc-S-benzyl-L-cysteine, 99%
Brand Name
J&K
Product Number
120799
CAS
5068-28-0
Molecular Formula
C15H21NO4S
Molecular Weight
311.40
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
Boc-S-benzyl-L-cysteine
PubChem CID
2724757
IUPAC Name
(2R)-3-benzylsulfanyl-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoic acid
InChI Key
IFVORPLRHYROAA-LBPRGKRZSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CSCC1=CC=CC=C1)C(=O)O

Properties

Melting Point
86-88
Optical Activity
-46° to -44° (C=1, AcOH)

Safety Information

Precautionary Statement
P262

References Data Source From Pubchem

Click chemistry modification of copolymers with cysteine amino acid: tunable thermal, electrical properties and kinetic analysis
Publication Name: Journal of Polymer Research
Publication Date: 2024-06
DOI: 10.1007/s10965-024-04014-3

Efficient and Practical Procedure for the Esterification of the Free α-Carboxylic Acid of Amino Acid Residues with β-(Trimethylsilyl)ethoxymethyl Chloride and Triisopropylsilyl Chloride
Publication Name: Synthesis
Publication Date: 2014-08-26
DOI: 10.1055/s-0034-1379004

Dipeptide derived from benzylcystine forms unbranched nanotubes in aqueous solution
Publication Name: Journal of Nanostructure in Chemistry
Publication Date: 2013-04-17
DOI: 10.1186/2193-8865-3-12

Design of silica microparticles with oligopeptide brushes and their interaction with proteins
Publication Name: Colloid and Polymer Science
Publication Date: 2010-11-03
DOI: 10.1007/s00396-010-2319-2

Synthesis and Characterization of Novel Organic/Inorganic Hybrid Material with Short Peptide Brushes Generated on the Surface
Publication Name: Biomacromolecules
Publication Date: 2007-08-22
DOI: 10.1021/bm700603q

Boc-S-benzyl-L-cysteine, 99%

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