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310565

Sigma-Aldrich

2-Phenylbenzoxazole

99%

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About This Item

Empirical Formula (Hill Notation):
C13H9NO
CAS Number:
833-50-1
Molecular Weight:
195.22
MDL number:
MFCD00012183
UNSPSC Code:
12352100
PubChem Substance ID:
24858803

Assay

99%

mp

102-104 °C (lit.)

functional group

phenyl

SMILES string

c1ccc(cc1)-c2nc3ccccc3o2

InChI

1S/C13H9NO/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9H

InChI key

FIISKTXZUZBTRC-UHFFFAOYSA-N

General description

2-Phenylbenzoxazole is present as a hydrophobic fluorospore in the fluorescent molecular sensors AS1-3[1]. The synthesis and microbiological activity of a new series of 5-benzamido- and 5-phenylacetamidosubstituted-2-phenylbenzoxazole derivatives were studied[2].

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

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
37797LJV
37797LJ
17706BA
12913KC
11529CY

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Jiaobing Wang et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(26), 7543-7552 (2007-06-22)
A series of amphiphilic intramolecular charge-transfer fluorescent molecular sensors AS1-3, equipped with a rod-shaped hydrophobic 2-phenylbenzoxazole fluorophore and a hydrophilic tetraamide Hg(2+)-ion receptor, have been prepared. These sensor molecules could be incorporated into the hydrophobic sodium dodecyl sulfate (SDS) micelle
E A Sener et al.
Farmaco (Societa chimica italiana : 1989), 55(5), 397-405 (2000-09-13)
The synthesis and microbiological activity of a new series of 5-benzamido- and 5-phenylacetamidosubstituted-2-phenylbenzoxazole derivatives (1-26) were described. The in vitro microbiological activity of the compounds was determined against Gram-positive, Gram-negative bacteria and the yeast Candida albicans in comparison with standard

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