A82605
11-氨基十一酸
97%
别名:
Aminoundecanoic acid
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关于此项目
线性分子式:
NH2(CH2)10CO2H
化学文摘社编号:
分子量:
201.31
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-417-6
Beilstein/REAXYS Number:
1767291
MDL number:
产品名称
11-氨基十一酸, 97%
InChI key
GUOSQNAUYHMCRU-UHFFFAOYSA-N
InChI
1S/C11H23NO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10,12H2,(H,13,14)
SMILES string
NCCCCCCCCCCC(O)=O
assay
97%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
color
white
mp
188-191 °C (lit.)
application(s)
peptide synthesis
Quality Level
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Application
111-氨基十一烷酸可作为linker合成酰胺连接的线性鸟苷二聚体。
General description
11-氨基十一烷酸，又称为氨基十一酸，常用于液相多肽合成法。还可用作尼龙11的单体前体。
存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Syntheses of 12-aminododecanoic and 11-aminoundecanoic acids from vernolic acid
Journal of the American Oil Chemists' Society, 74, 531-538 (1997)
Development of Minimal Diguanosinyl Motif toward RNA G-Quadruplex-Like Structures in Solution
Chembiochem, 21, 1837-1842 (2020)
P Kyprianou et al.
The Biochemical journal, 207(3), 549-556 (1982-12-01)
1. The theory of Nichol, Ogston, Winzor & Sawyer [(1974) Biochem. J. 143, 435-443] for quantitative affinity chromatography, when adapted for use with a non-specific column from which a multi-site protein can be specifically desorbed by its free ligand, permits
M Marastoni et al.
European journal of medicinal chemistry, 35(6), 593-598 (2000-07-25)
The latent membrane protein 2 (LMP2) is expressed in EBV-associated tumours. LMP2 is a target of HLA-A2 restricted EBV-specific CTL responses and consequently it may represent a good target for specific CTL-based immunotherapies. However, the efficacy of such therapy is
Liling Zeng et al.
Nano letters, 5(10), 2001-2004 (2005-10-13)
Carboxylic acid-functionalized SWNTs prepared via the reaction of an amino acid, NH2(CH2)nCO2H, with fluoronanotubes show similar levels of sidewall functionalization; however, the solubility in water is controlled by the length of the hydrocarbon side chain (i.e., n). The 6-aminohexanoic acid
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