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C9004

Z-DL-Ser-OH

Name: Z-<SC>DL</SC>-Ser-OH
Brand: ALDRICH

99%

Synonym(s):

N-Cbz-DL-serine

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About This Item

Linear Formula:

HOCH₂CH(NHCO₂CH₂C₆H₅)CO₂H

CAS Number:

2768-56-1

Molecular Weight:

239.22

UNSPSC Code:

12352209

NACRES:

NA.22

PubChem Substance ID:

24893124

EC Number:

220-455-0

Beilstein/REAXYS Number:

3593625

MDL number:

MFCD00063143

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Properties

assay

99%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

color

white

mp

124-126 °C (lit.)

application(s)

peptide synthesis

SMILES string

OCC(NC(=O)OCc1ccccc1)C(O)=O

InChI

1S/C11H13NO5/c13-6-9(10(14)15)12-11(16)17-7-8-4-2-1-3-5-8/h1-5,9,13H,6-7H2,(H,12,16)(H,14,15)

InChI key

GNIDSOFZAKMQAO-UHFFFAOYSA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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(R)-tert-Butoxycarbonylamino-fluorenylmethoxycarbonyl-glycine from (S)-benzyloxycarbonyl-serine or from papain resolution of the corresponding amide or methyl ester.

M Sypniewski et al.

The Journal of organic chemistry, 65(20), 6595-6600 (2000-10-29)

The enantiospecific synthesis of (R)-Boc-(Fmoc)-aminoglycine 7 was achieved. (S)-Cbz-serine 1 was reacted with diphenylphosphoryl azide in the presence of triethylamine to yield cyclic (S) carbamate 2. The ring nitrogen of 2 was protected with a Boc group (3). The cyclic

Analyte separation by OMNiMIPs imprinted with multiple templates.

Jason Lejeune et al.

Biosensors & bioelectronics, 25(3), 604-608 (2009-03-27)

Changes detected in the imprinting effect by OMNiMIPs imprinted with multiple templates appear to be a function of the maximum template loading. Below the maximum template loading, the polymers imprinted with multiple compounds provide molecular recognition close to the polymers

Global Trade Item Number

SKU	GTIN
C9004-25G	04061832644837