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542873

Sigma-Aldrich

Pyrene-1-boronic acid

≥95.0%

Synonym(s):

1-Pyreneboronic acid, 1-Pyrenylboronic acid

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About This Item

Empirical Formula (Hill Notation):
C16H11BO2
CAS Number:
164461-18-1
Molecular Weight:
246.07
MDL number:
MFCD04974062
UNSPSC Code:
12352103
PubChem Substance ID:
24878642
NACRES:
NA.22

Assay

≥95.0%

form

solid

mp

247-251 °C (lit.)

SMILES string

OB(O)c1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C16H11BO2/c18-17(19)14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9,18-19H

InChI key

MWEKPLLMFXIZOC-UHFFFAOYSA-N

Related Categories

Other Notes

Contains varying amounts of anhydride

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN5079
SHBK4657
SHBH0774V
SHBB2013V
28796BM

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Mohamed E El-Khouly et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 16(10), 1512-1518 (2017-08-02)
A light harvesting subphthalocyanine-pyrene dyad has been synthesized and characterized by linking pyrene (Py) with subphthalocyanine (SubPc) at its axial position with the B-O bond through the para position of the benzene group. Upon photoexcitation at the pyrene unit of
Hailei Zhang et al.
ACS applied materials & interfaces, 7(42), 23805-23811 (2015-10-10)
A novel fluorescence probe based on modified halloysite nanotubes (HNTs) by using 1-pyrenylboronic acid selectively grafted onto the inner surface of lumen was successfully achieved. The solid-state nuclear magnetic resonance ((13)C and (11)B), X-ray photoelectron spectroscopy (XPS) and Fourier transform

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