C9004
Z-DL-Ser-OH
99%
Synonym(s):
N-Cbz-DL-serine
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About This Item
Linear Formula:
HOCH2CH(NHCO2CH2C6H5)CO2H
CAS Number:
Molecular Weight:
239.22
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-455-0
Beilstein/REAXYS Number:
3593625
MDL number:
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
SMILES string
OCC(NC(=O)OCc1ccccc1)C(O)=O
assay
99%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
color
white
mp
124-126 °C (lit.)
application(s)
peptide synthesis
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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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
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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