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Merck

392189

Sigma-Aldrich

1-Pyreneacetic acid

97%

Sinónimos:

(1-Pyrenyl)acetic acid

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About This Item

Fórmula empírica (notación de Hill):
C18H12O2
Número de CAS:
Peso molecular:
260.29
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

form

solid

mp

210-212 °C (dec.) (lit.)

functional group

carboxylic acid

SMILES string

OC(=O)Cc1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C18H12O2/c19-16(20)10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)18(13)17(11)12/h1-9H,10H2,(H,19,20)

InChI key

SDJCLYBBPUHKCD-UHFFFAOYSA-N

General description

1-Pyreneacetic acid is a negatively charged pyrene derivative. It has been proposed as titrating reagent for the standardization titration of Grignard reagents and n-butyl lithium (n-BuLi).

Application

1-Pyreneacetic acid is suitable for use in the following studies:
  • Synthesis of N-(2-(methylthio)ethyl)-2-(pyren-1-yl)acetamide, a pyrene amide based Pd2+ probe.
  • Synthesis of pyrene-modified β-cyclodextrin.
  • To functionalize single walled carbon nanotube field effect transistors (CNT FETs).
  • As an agent for characterizing grafting degrees and reactivity of the ester functionalized polypropylenes.
  • Synthesis sawhorse-type diruthenium tetracarbonyl complexes.
  • Synthesis of (±)-2-(1-pyrenyl)propionic acid, a chiral carboxylic acid.
  • Reversible noncovalent functionalization of single walled carbon nanotubes (SWNTs).
  • Preparation of peptide nucleic acid (PNA) probes.
  • As an internal reference compound in the assessment of solid phase reaction by HPLC-UV.

Storage Class

11 - 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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Visite la Librería de documentos

Kadish KM, et al.
Handbook of Porphyrin Science: With Applications to Chemistry, Physics, Materials Science, Engineering, Biology and Medicine, Volumes 1-5, 1-5, 107-107 (2010)
Mitchell B Lerner et al.
Journal of the American Chemical Society, 134(35), 14318-14321 (2012-08-17)
Despite the great promise of carbon nanotube field-effect transistors (CNT FETs) for applications in chemical and biochemical detection, a quantitative understanding of sensor responses is lacking. To explore the role of electrostatics in sensor transduction, experiments were conducted with a
Ester functionalization of polypropylene via controlled decomposition of benzoyl peroxide during solid-state shear pulverization.
Diop MF and Torkelson JM.
Macromolecules, 46(19), 7834-7844 (2013)
Rappoport Z and Marek I.
The Chemistry of Organomagnesium Compounds, 288-288 (2008)
Thioether Amide Based-Fluorescent Chemosensors for Pd2+ with High Selectivity over Pd 0.
Ahn SY, et al.
Bull. Korean Chem. Soc., 35(7), 2189-2189 (2014)

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