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446300

Sigma-Aldrich

2-Phenylindene

97%

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About This Item

Empirical Formula (Hill Notation):
C15H12
CAS Number:
Molecular Weight:
192.26
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

mp

157-161 °C (lit.)

SMILES string

C1c2ccccc2C=C1c3ccccc3

InChI

1S/C15H12/c1-2-6-12(7-3-1)15-10-13-8-4-5-9-14(13)11-15/h1-10H,11H2

InChI key

BSBXLZYWGGAVHD-UHFFFAOYSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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Chemical behavior of o-bis (phenylethynyl) benzene toward some electrophilic and nucleophilic reagents.
Whitlock Jr HW, et al.
The Journal of Organic Chemistry, 34(4), 879-886 (1969)
Christian Müller et al.
The journal of physical chemistry. A, 110(15), 5017-5031 (2006-04-14)
We investigated the spectroscopy of the first excited singlet electronic state S1 of 2-phenylindene using both fluorescence excitation spectroscopy and resonantly enhanced multiphoton ionization spectroscopy. Moreover, we investigated the dynamics of the S1 state by determining state-selective fluorescence lifetimes up
Ozonolyses of 1, 2-diphenyl-and 2-phenylindene.
Sugimoto T, et al.
The Journal of Organic Chemistry, 58(1), 135-141 (1993)
Observation of intramolecular vibrational redistribution and vibrational cooling in S 1 trans-stilbene and 2-phenylindene in solution.
Qian J, et al.
Chemical Physics Letters, 233(1), 9-15 (1995)
A convenient synthesis of 2-arylindenes.
Bendall VI and Dharamshi SS.
Journal of the Chemical Society. Perkin Transactions 1, 2732-2734 (1972)

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