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trans-N-Cbz-4-hydroxy-L-proline, 98%|999380|13504-85-3

trans-N-Cbz-4-hydroxy-L-proline, 98%

Cat. No JK999380_25_G
J&K Chemical

Product Information

Product Name
trans-N-Cbz-4-hydroxy-L-proline, 98%
Brand Name
J&K
Product Number
999380
CAS
13504-85-3
Molecular Formula
C13H15NO5
Molecular Weight
265.27
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
Z-Hyp-OH
PubChem CID
391517
IUPAC Name
(2S,4R)-4-hydroxy-1-phenylmethoxycarbonylpyrrolidine-2-carboxylic acid
InChI Key
WWVCWLBEARZMAH-MNOVXSKESA-N
SMILES
C1C@H(CN(C@@H1C(=O)O)C(=O)OCC2=CC=CC=C2)O

Properties

Melting Point
104-107
Optical Activity
-53° to -56° (C=2, EtOH)

References Data Source From Pubchem

New chiral proline-based catalysts for silicon and zirconium oxides-promoted asymmetric Biginelli reaction
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2018-04
DOI: 10.1007/s10593-018-2285-z

Synthesis of HCV Protease Inhibitor MK-1220
Publication Name: Synfacts
Publication Date: 2014-05-16
DOI: 10.1055/s-0033-1341262

Silica-immobilized N,O-prolinate ruthenium benzylidene complexes for catalytic applications
Publication Name: Journal of Sol-Gel Science and Technology
Publication Date: 2011-10-20
DOI: 10.1007/s10971-011-2610-9

Dimeric Cationic Amphiphilic Polyproline Helices for Mitochondrial Targeting
Publication Name: Pharmaceutical Research
Publication Date: 2011-06-07
DOI: 10.1007/s11095-011-0493-7

A Novel and Facile One-Pot Method for the Synthesis of N-Substituted Sulfamates
Publication Name: Synthesis
Publication Date: 2008-07
DOI: 10.1055/s-2008-1067156

trans-N-Cbz-4-hydroxy-L-proline, 98%

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