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17852

Sigma-Aldrich

4-(Boc-amino)-1-methylpyrrole-2-carboxylic acid

≥99.0% (HPLC)

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About This Item

Empirical Formula (Hill Notation):
C11H16N2O4
CAS Number:
Molecular Weight:
240.26
Beilstein/REAXYS Number:
4470648
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

assay

≥99.0% (HPLC)

form

solid

mp

156-160 °C (dec.)

application(s)

peptide synthesis

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

Other Notes

Unnatural amino acid for preparing heteroaromatic oligoamides for regulating gen expression in biotechnology[1][2]

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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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