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105481

Sigma-Aldrich

1,3-Diphenylisobenzofuran

97%

Synonym(s):

1,3-Diphenyl-2-benzofuran, 2,5-Diphenyl-3,4-benzofuran

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About This Item

Empirical Formula (Hill Notation):
C20H14O
CAS Number:
5471-63-6
Molecular Weight:
270.32
Beilstein:
199922
EC Number:
226-808-5
MDL number:
MFCD00005931
UNSPSC Code:
12352100
PubChem Substance ID:
24846701
NACRES:
NA.22

Assay

97%

form

solid

mp

128-130 °C (lit.)

functional group

phenyl

SMILES string

c1ccc(cc1)-c2oc(-c3ccccc3)c4ccccc24

InChI

1S/C20H14O/c1-3-9-15(10-4-1)19-17-13-7-8-14-18(17)20(21-19)16-11-5-2-6-12-16/h1-14H

InChI key

ZKSVYBRJSMBDMV-UHFFFAOYSA-N

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General description

1,3-Diphenylisobenzofuran is a fluorescent dye.1,3-Diphenylisobenzofuran is the model compound in studies of singlet fission.

Application

1,3-Diphenylisobenzofuran(DPBF) was used as a fluorescent probe for detection of superoxide anion radical (O2−) inside the membrane lipid layer by DPBF fluorescence quenching method. 1,3-Diphenylisobenzofuran(DPBF) was used as quencher during the photoinactivation of TA-3 mouse mammary carcinoma cells containing hematoporphyrin. 1,3-Diphenylisobenzofuran(DPBF) was used to study the single crystal molecular structure and solution photophysical properties of DPBF.

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Zhihao Han et al.
Journal of biophotonics, 10(12), 1607-1616 (2017-01-21)
It is an emerging focus to explore controlled release drug delivery systems for simultaneous cancer imaging and therapy. Herein, we synthesized a photothermal sensitive multifunctional nano-liposome drug delivery system, with doxorubicin wrapped in the hydropholic layer as the therapeutical agent
Huanhuan Liu et al.
Scientific reports, 9(1), 8393-8393 (2019-06-12)
A great number of fluorescent probes have been developed for detecting singlet oxygen (1O2), which is considered to be one of the most effective reactive oxygen species (ROS), especially in clinical applications. The commercially available fluorescent probe Singlet Oxygen Sensor
Andrew F Schwerin et al.
The journal of physical chemistry. A, 114(3), 1457-1473 (2009-12-23)
Single crystal molecular structure and solution photophysical properties are reported for 1,3-diphenylisobenzofuran (1), of interest as a model compound in studies of singlet fission. For the ground state of 1 and of its radical cation (1(+*)) and anion (1(-*)), we
Xumei Ouyang et al.
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