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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

Beilstein:

3593625

EC Number:

220-455-0

MDL number:

MFCD00063143

UNSPSC Code:

12352209

PubChem Substance ID:

24893124

NACRES:

NA.22

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

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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

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