Key Documents

View All Documentation

C8601

Z-Pro-OH

Name: Z-Pro-OH
Brand: ALDRICH

99%

Synonym(s):

Z-L-Proline

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₁₃H₁₅NO₄

CAS Number:

1148-11-4

Molecular Weight:

249.26

NACRES:

NA.22

PubChem Substance ID:

24893080

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

214-557-4

MDL number:

MFCD00003170

Beilstein/REAXYS Number:

88579

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

200

assay

99%

form

powder or crystals

optical activity

[α]20/D −42°, c = 2 in ethanol

reaction suitability

reaction type: solution phase peptide synthesis

technique(s)

NMR: suitable

color

white

mp

76-78 °C (lit.)

application(s)

peptide synthesis

SMILES string

OC(=O)[C@@H]1CCCN1C(=O)OCc2ccccc2

InChI

1S/C13H15NO4/c15-12(16)11-7-4-8-14(11)13(17)18-9-10-5-2-1-3-6-10/h1-3,5-6,11H,4,7-9H2,(H,15,16)/t11-/m0/s1

InChI key

JXGVXCZADZNAMJ-NSHDSACASA-N

Description

Application

Z-Pro-OH can be used:

As a starting material to prepare aib-pro endothiopeptides of pharmacological importance.
To prepare biologically significant fluorophore-labeled peptide tetramers or dimers.
As a reactant to synthesize benzoxazole derived human neutrophil elastase (HNE) inhibitors.

ppe

Eyeshields, Gloves, type N95 (US)

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

A new dendrimer scaffold for preparing dimers or tetramers of biologically active molecules

Raju N, et al.

Tetrahedron Letters, 46(9), 1463-1465 (2005)

Design and synthesis of peptide-based carboxylic acid-containing transition-state inhibitors of human neutrophil elastase

Sato F, et al.

Bioorganic & medicinal chemistry letters, 12(4), 551-555 (2002)

The `azirine/oxazolone approach?to the synthesis of Aib-Pro endothiopeptides

Budzowski A, et al.

Helvetica Chimica Acta, 91(8), 1471-1488 (2008)

View All Related Papers

Global Trade Item Number

SKU	GTIN
C8601-10G	04061833522585