20589
O-叔丁基-L-丝氨酸叔丁酯 盐酸盐
≥98.0% (AT)
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关于此项目
经验公式（希尔记法）:
C11H23NO3 · HCl
化学文摘社编号:
分子量:
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
保护性 L-丝氨酸，用于多肽合成，例如糖肽和脂肽的合成；也可用于氨基磷脂的制备
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
H. Paulsen et al.
Liebigs Ann. Chem., 751-751 (1989)
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.
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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