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trans-Stilbene
trans-Stilbene
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name trans-Stilbene
Price: $30 / 20mg
CAS No.: 103-30-0
Catalog No.: CFN70005
Molecular Formula: C14H12
Molecular Weight: 180.2 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Source:
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
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Biological Activity
Description: Reference standards.
trans-Stilbene Description
Source:
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.5494 mL 27.7469 mL 55.4939 mL 110.9878 mL 138.7347 mL
5 mM 1.1099 mL 5.5494 mL 11.0988 mL 22.1976 mL 27.7469 mL
10 mM 0.5549 mL 2.7747 mL 5.5494 mL 11.0988 mL 13.8735 mL
50 mM 0.111 mL 0.5549 mL 1.1099 mL 2.2198 mL 2.7747 mL
100 mM 0.0555 mL 0.2775 mL 0.5549 mL 1.1099 mL 1.3873 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Macromolecular Chemistry & Physics, 1995, 196(6):1999-2009.
Complex‐radical alternating terpolymerization of maleic anhydride, trans-stilbene and N-phenylmaleimide.[Reference: WebLink]

METHODS AND RESULTS:
Radical terpolymerizations of maleci anhydride (MA), trans-Stilbene (Stb) and N-phenylmale-imide (PhMI) were carried out in methyl ethyl ketone (MEK) at 60-80 C in the presence of 2,2'-azoisobutyronitrile (AIBN) as initiator. The terpolymerization was evaluated by using either the free monomer or complex participation models. The relative of MA toward poly(Stb) radical was found to be about 10,6 times lower than that of PhMl. The initial rate of copolymerization, the participation of the charge transfer complex (CTC) monomers and free monomers was quantitatively estimated. It was established that, even with a considerable change in the ratio of electron-acceptor monomers (MA and PhMI) in the initial reaction mixture, terpolymers possessed always a composition ratio close to 1:2:1. Constants for copolymerization of MA-Stb (M1) and PhMI-Stb (M3) were determined by using the Kelen-Tudos equation, and r1 . K1/K3 = 0,03 and r2 . K3/1 =0,08, where K1 and K3 are complex-formation constants of MA-Stb and PhMl-Stb complexes, respectively, were obtained.
CONCLUSIONS:
The result of kinetic studies of terpolymerization was interpreted as involving mainly alternating copolymerization of two complexomers with predominant participation in chain growth. Thermogravimetric analyses indicated the high thermal stabilities of terpolymers obtained.
Journal of Photochemistry & Photobiology A Chemistry, 1995, 85(3):225-229.
Solid state photoaddition reactions in polycrystalline mixtures of NH heteroaromatic compounds and trans-stilbene.[Reference: WebLink]

METHODS AND RESULTS:
Photoaddition reactions of indole ( 1a ), carbazole ( 1b ) and phenothiazine ( 1c ) to trans -stilbene ( 2 ) occurred in the mixed crystal state to give the corresponding adducts 3a , 3b and 3c with an N C bond. Photoadduct 4a with a C C bond was also obtained by the solid state photoreaction of 1a with 2 . The mixed crystals prepared by the melting and resolidifying method were simple polycrystalline mixtures of the two components, and the photoreactions proceeded at the interface of the two crystallites.
CONCLUSIONS:
The selectivity of the photoaddition reaction was higher in the solid state than in solution.
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