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
Beilstein:
4886392
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22
方案
≥98.0% (AT)
表单
solid
旋光性
[α]/D -10.0±1.0°, c = 1 in H2O
反应适用性
reaction type: solution phase peptide synthesis
应用
peptide synthesis
SMILES字符串
Cl.CC(C)(C)OC[C@H](N)C(=O)OC(C)(C)C
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
InChI key
RDWZQVGVBTYCBD-QRPNPIFTSA-N
其他说明
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
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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)
Liebigs Ann. Chem., 771-771 (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
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