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经验公式(希尔记法):
C11H16N2O4
化学文摘社编号:
分子量:
240.26
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
4470648
MDL number:
SMILES string
Cn1cc(NC(=O)OC(C)(C)C)cc1C(O)=O
InChI
1S/C11H16N2O4/c1-11(2,3)17-10(16)12-7-5-8(9(14)15)13(4)6-7/h5-6H,1-4H3,(H,12,16)(H,14,15)
InChI key
GOLAEMFBWAIGRX-UHFFFAOYSA-N
assay
≥99.0% (HPLC)
form
solid
mp
156-160 °C (dec.)
application(s)
peptide synthesis
Other Notes
用于制备在生物技术中调节基因表达所需杂环芳族低聚酰胺的非天然氨基酸
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
E.E. Baird et al.
Journal of the American Chemical Society, 118, 6141-6141 (1996)
S White et al.
Nature, 391(6666), 468-471 (1998-02-14)
The design of synthetic ligands that read the information stored in the DNA double helix has been a long-standing goal at the interface of chemistry and biology. Cell-permeable small molecules that target predetermined DNA sequences offer a potential approach for
Karine Nozeret et al.
Biochimie, 149, 122-134 (2018-04-08)
Pericentromeric heterochromatin plays important roles in controlling gene expression and cellular differentiation. Fluorescent pyrrole-imidazole polyamides targeting murine pericentromeric DNA (major satellites) can be used for the visualization of pericentromeric heterochromatin foci in live mouse cells. New derivatives targeting human repeated
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