225444
2-Phenylbenzothiazole
97%
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About This Item
Empirical Formula (Hill Notation):
C13H9NS
CAS Number:
Molecular Weight:
211.28
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-935-3
MDL number:
Assay:
97%
Form:
solid
Product Name
2-Phenylbenzothiazole, 97%
InChI key
XBHOUXSGHYZCNH-UHFFFAOYSA-N
InChI
1S/C13H9NS/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9H
SMILES string
c1ccc(cc1)-c2nc3ccccc3s2
assay
97%
form
solid
mp
111-113 °C (lit.)
functional group
phenyl
Quality Level
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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
11 - Combustible Solids
wgk
WGK 3
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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
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).
Stamatia Tzanopoulou et al.
Inorganic chemistry, 45(2), 902-909 (2006-01-18)
The reaction of 2-(2'-pyridyl)benzothiazole, [NN], with the ReO(V)(3+) and TcO(V)(3+) cores in the presence of thiophenols, [S] (RC(6)H(4)SH, R = H, 4-CH(3), 4-OCH(3)), as coligands led to the isolation of hexacoordinated complexes of the MO[NN][S](3) type (M = Re, Tc).
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
P Ivanov et al.
Journal of fluorescence, 22(6), 1501-1507 (2012-07-10)
The parent study includes synthesis end photophysical characterization of four new phosphorescent cyclometalated iridium (III) complexes. The cyclometaled ligands used here are 2-(4-chlorophenyl)benzo[d]thiazole, 2(4isopropylphenyl)benzo[d] thiazole, 2-(4-methoxyphenyl)benzo[d]thiazole, 4-(benzo[d]thiazol-2-yl)-N,N-dimethylaniline. The auxiliary ligand is acetylacetone (Hacac). The photometric analyses show temperature dependence on
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