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Merck
CN

139939

trans-Stilbene

96%

Synonym(s):

trans-1,2-Diphenylethylene

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About This Item

Linear Formula:
C6H5CH=CHC6H5
CAS Number:
103-30-0
Molecular Weight:
180.25
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
24848441
EC Number:
203-098-5
Beilstein/REAXYS Number:
1616740
MDL number:
MFCD00064300

Key Documents

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InChI key

PJANXHGTPQOBST-VAWYXSNFSA-N

InChI

1S/C14H12/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-12H/b12-11+

SMILES string

c1ccc(cc1)\C=C\c2ccccc2

assay

96%

form

solid

bp

305-307 °C/744 mmHg (lit.)

Quality Level

100

Gene Information

human ... ESR1(2099)
rat ... Esr1(24890)

density

0.97 g/mL at 25 °C (lit.)

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Application

Commonly employed in transition metal catalyzed asymmetric epoxidation and dihydroxylation.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP1851
BCCM8050
BCCL2685
BCCJ9278
BCCH7379

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The effect of material purity on the optical and scintillation properties of solution-grown trans-stilbene crystals
Carman, Leslie, et al.
Journal of Crystal Growth, 368, 56-61 (2013)
Tetrahedron Letters, 33, 4021-4021 (1992)
Miłosz Regulski et al.
Bioorganic & medicinal chemistry, 26(1), 141-151 (2017-12-02)
25 new trans-stilbene and trans-stilbazole derivatives were investigated using in vitro and in silico techniques. The selectivity and potency of the compounds were assessed using commercial ELISA test. The obtained results were incorporated into 2D QSAR assay. The most promising
Conformational information from vibrational spectra of styrene, trans-stilbene, and cis-stilbene.
Choi, Cheol Ho, and Miklos Kertesz
The Journal of Physical Chemistry A, 101(20), 3823-3831 (1997)
Ujjal Bhattacharjee et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 18(18), 2526-2532 (2017-07-12)
The ability to produce large-scale, reversible structural changes in a variety of materials by photoexcitation of a wide variety of azobenzene derivatives has been recognized for almost two decades. Because photoexcitation of trans-azobenzene produces the cis-isomer in solution, it has
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