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Sigma-Aldrich

2-Phenylbenzothiazole

97%

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About This Item

Empirical Formula (Hill Notation):
C13H9NS
CAS Number:
Molecular Weight:
211.28
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

111-113 °C (lit.)

SMILES string

c1ccc(cc1)-c2nc3ccccc3s2

InChI

1S/C13H9NS/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9H

InChI key

XBHOUXSGHYZCNH-UHFFFAOYSA-N

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Application

2-Phenylbenzothiazole was used in the synthesis of two novel orange iridium(III) complexes, (bis[2-(biphenyl-3-yl)benzothiazole-N,C2′]iridium(III)(acetylacetonate) and bis[2-(4′-methoxybiphenyl-3-yl)benzothiazole-N,C2′]iridium(III) (acetylacetonate).

Storage Class Code

11 - Combustible Solids

WGK

WGK 3


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Kuo-Shyan Lin et al.
Bioorganic & medicinal chemistry letters, 19(8), 2258-2262 (2009-03-17)
As a first step toward the development of (99m)Tc PiB analogs, we have synthesized six neutral Re 2-phenylbenzothiazoles via pendant or integrated approach. These Re compounds bind to Abeta(1-40) fibrils with fairly good affinities (K(i)=10.0-88.6nM) and have moderate lipophilicities (logP(C18)=1.21-3.26).
Rahmi Imamoglu et al.
Nature communications, 11(1), 365-365 (2020-01-19)
The ATP-dependent Hsp70 chaperones (DnaK in E. coli) mediate protein folding in cooperation with J proteins and nucleotide exchange factors (E. coli DnaJ and GrpE, respectively). The Hsp70 system prevents protein aggregation and increases folding yields. Whether it also enhances
Rupam Sarma et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 77(1), 126-129 (2010-06-16)
The UV-visible and fluorescence properties of hydroxy substituted benzothiazole derivatives change on interactions with zinc(II), cadmium(II) and mercury(II) ions. The binding of 2-(2'-hydroxyphenyl)benzothiazole is specific to zinc(II) over cadmium(II) and mercury(II). Similar type of interactions of zinc(II), cadmium(II) and mercury(II)
Jun Dai et al.
Dalton transactions (Cambridge, England : 2003), 42(29), 10559-10571 (2013-06-14)
By introducing a phenyl substituent into the meta-site of the phenyl segment of the 2-phenylbenzothiazole ligand, two novel orange iridium(III) complexes, namely, (3Phbt)2Ir(acac) and (3OMePhbt)2Ir(acac), have been synthesized. Compared with their parent compound (bt)2Ir(acac), both of them possess much enhanced
Ming Li et al.
Dalton transactions (Cambridge, England : 2003), 40(27), 7153-7164 (2011-06-15)
Four novel iridium(III) complexes bearing biphenyl (7a-7c) or fluorenyl (7d) modified benzothiazole cyclometallate ligands are synthesized. In comparison with the yellow parent complex, bis(2-phenylbenzothiozolato-N,C(2')) iridium(III) (acetylacetonate) [(pbt)(2)Ir(acac)] (λ(PLmax) = 557 nm, φ(PL) = 0.26), 7a-7d show 20-43 nm bathochromic shifted

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