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Safety Information

C9004

Sigma-Aldrich

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:
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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

C9004-25G:
C9004-BULK:
C9004-VAR:
C9004-10G:

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Certificates of Analysis (COA)

Lot/Batch Number
23121PI
1720DO
16718JI
15630TQ
13204HO

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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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