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139939

Sigma-Aldrich

trans-Stilbene

96%

Synonym(s):

trans-1,2-Diphenylethylene

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About This Item

Linear Formula:
C6H5CH=CHC6H5
CAS Number:
Molecular Weight:
180.25
Beilstein:
1616740
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Assay

96%

form

solid

bp

305-307 °C/744 mmHg (lit.)

mp

123-125 °C (lit.)

density

0.97 g/mL at 25 °C (lit.)

SMILES string

c1ccc(cc1)\C=C\c2ccccc2

InChI

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

InChI key

PJANXHGTPQOBST-VAWYXSNFSA-N

Gene Information

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

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Application

Commonly employed in transition metal catalyzed asymmetric epoxidation and dihydroxylation.

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Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

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

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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Synlett, 407-407 (1992)
The effect of material purity on the optical and scintillation properties of solution-grown trans-stilbene crystals
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Journal of Crystal Growth, 368, 56-61 (2013)
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
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

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