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About This Item
线性分子式:
(CH3)3CO2CNH(CH2)5CO2H
CAS号:
分子量:
231.29
Beilstein:
2049561
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.22
质量水平
检测方案
≥99.0% (T)
形式
solid
反应适用性
reaction type: Boc solid-phase peptide synthesis
mp
35-40 °C
应用
peptide synthesis
储存温度
2-8°C
SMILES字符串
CC(C)(C)OC(=O)NCCCCCC(O)=O
InChI
1S/C11H21NO4/c1-11(2,3)16-10(15)12-8-6-4-5-7-9(13)14/h4-8H2,1-3H3,(H,12,15)(H,13,14)
InChI key
RUFDYIJGNPVTAY-UHFFFAOYSA-N
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相关类别
其他说明
引入 ε 的保护衍生物各种化合物中的 -氨基己基部分。 在亲和层析中引入氨基己酸间隔臂。
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Affinity chromatography of carboxypeptidase B.
M Sokolovsky
Methods in enzymology, 34, 411-414 (1974-01-01)
A J Schroit et al.
Biochemistry, 22(15), 3617-3623 (1983-07-19)
An efficient method for the synthesis and purification of a variety of iodinated phospholipid analogues is described. 1-Acyl-2-[[[3-(3-[125I]iodo-4-hydroxyphenyl)- propionyl]amino]caproyl]phosphatidylcholine (125I-PC) was prepared by alkylation of 1-acyl-2-(aminocaproyl)phosphatidylcholine with monoiodinated Bolton-Hunter reagent. 125I-Labeled phosphatidic acid, phosphatidylethanolamine, and phosphatidylserine were produced from 125I-PC
The literature on affinity chromatography.
M Wilchek et al.
Methods in enzymology, 34, 3-10 (1974-01-01)
J. Frank et al.
Helvetica Chimica Acta, 60, 2550-2550 (1977)
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