20589
O-tert-Butyl-L-serine tert-butyl ester hydrochloride
≥98.0% (AT)
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About This Item
Empirical Formula (Hill Notation):
C11H23NO3 · HCl
CAS Number:
Molecular Weight:
253.77
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4886392
InChI
1S/C11H23NO3.ClH/c1-10(2,3)14-7-8(12)9(13)15-11(4,5)6;/h8H,7,12H2,1-6H3;1H/t8-;/m0./s1
SMILES string
Cl.CC(C)(C)OC[C@H](N)C(=O)OC(C)(C)C
InChI key
RDWZQVGVBTYCBD-QRPNPIFTSA-N
assay
≥98.0% (AT)
form
solid
optical activity
[α]/D -10.0±1.0°, c = 1 in H2O
reaction suitability
reaction type: solution phase peptide synthesis
application(s)
peptide synthesis
Other Notes
Protected L-serine used in peptide synthesis, e.g. synthesis of glycopeptides and lipopeptides; Preparation of amino-phospholipids
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Y Tsuda et al.
Chemical & pharmaceutical bulletin, 39(3), 607-611 (1991-03-01)
The structure of WS1279, isolated from Streptomyces sp. as an immunoactive lipopeptide, has been deduced on the basis of chemical and physical evidence as S-[2,3-bis(palmitoyloxy)propyl]-N alpha-palmitoyl-Cys-Asn-Ser-Gly-Gly-Ser- OH. This was confirmed by synthesis.
H. Paulsen et al.
Liebigs Ann. Chem., 751-751 (1989)
J G Turcotte et al.
Chemistry and physics of lipids, 58(1-2), 81-95 (1991-05-01)
A homologous series of chiral (R) ether-amide phosphonolipid analogs of naturally occurring (R) glycerophospholipids were synthesized and characterized for their interfacial behaviors. The phosphonolipids possess isoteric ether, amide, and phosphonate functions at positions corresponding to the sn-1, sn-2, and sn-3
Liebigs Ann. Chem., 771-771 (1989)
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