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Merck
CN

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:
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Quality Level

assay

97%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

color

white

mp

188-191 °C (lit.)

application(s)

peptide synthesis

SMILES string

NCCCCCCCCCCC(O)=O

InChI

1S/C11H23NO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10,12H2,(H,13,14)

InChI key

GUOSQNAUYHMCRU-UHFFFAOYSA-N

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。

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。


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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)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Development of Minimal Diguanosinyl Motif toward RNA G-Quadruplex-Like Structures in Solution
Chembiochem, 21, 1837-1842 (2020)
Syntheses of 12-aminododecanoic and 11-aminoundecanoic acids from vernolic acid
Journal of the American Oil Chemists' Society, 74, 531-538 (1997)
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



全球贸易项目编号

货号GTIN
A82605-500G04061832596914
A82605-100G04061833391365