1,3-DICHLORO-5-[(1E)-2(4-TRIFLUOROMETHYLPHENYL)ETHENYL]-BENZENE
- Product Name
- 1,3-DICHLORO-5-[(1E)-2(4-TRIFLUOROMETHYLPHENYL)ETHENYL]-BENZENE
- CAS No.
- 688348-33-6
- Chemical Name
- 1,3-DICHLORO-5-[(1E)-2(4-TRIFLUOROMETHYLPHENYL)ETHENYL]-BENZENE
- Synonyms
- CAY10465;CAY10465 Exclusive;CAY 10465, 10 mM in DMSO;CAY10465;CAY-10465;CAY 10465;1,3-Dichloro-5-(4-(trifluoromethyl)styryl)benzene;1,3-DICHLORO-5-[(1E)-2(4-TRIFLUOROMETHYLPHENYL)ETHENYL]-BENZENE;1,3-dichloro-5-{(E)-2-[4-(trifluoromethyl)phenyl]ethenyl}benzene;CAY-10465,AhR,CAY 10465,inhibit,Inhibitor,Aryl Hydrocarbon Receptor;Benzene, 1,3-dichloro-5-[(1E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-
- CBNumber
- CB1397651
- Molecular Formula
- C15H9Cl2F3
- Formula Weight
- 317.13
- MOL File
- Mol file
1,3-DICHLORO-5-[(1E)-2(4-TRIFLUOROMETHYLPHENYL)ETHENYL]-BENZENE Property
- Boiling point:
- 361.2±42.0 °C(Predicted)
- Density
- 1.378±0.06 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMF: 30 mg/ml; DMSO: 30 mg/ml; DMSO:PBS (pH 7.2)(1:1): .5 mg/ml; Ethanol: 20 mg/ml
- form
- A crystalline solid
- color
- White to off-white
N-Bromosuccinimide Price
- Product number
- 10006546
- Product name
- CAY10465
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $22
- Updated
- 2024/03/01
- Product number
- 10006546
- Product name
- CAY10465
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $95
- Updated
- 2024/03/01
- Product number
- 10006546
- Product name
- CAY10465
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $167
- Updated
- 2024/03/01
- Product number
- 10006546
- Product name
- CAY10465
- Purity
- ≥98%
- Packaging
- 50mg
- Price
- $723
- Updated
- 2024/03/01
- Product number
- T790970
- Product name
- (E)-1-[4-(Trifluoromethyl)phenyl]-2-(3,5-dichlorophenyl)ethene
- Packaging
- 1mg
- Price
- $85
- Updated
- 2021/12/16
1,3-DICHLORO-5-[(1E)-2(4-TRIFLUOROMETHYLPHENYL)ETHENYL]-BENZENE Chemical Properties,Usage,Production
Description
The aryl hydrocarbon receptor (AhR) is a ligand-
Uses
(E)-1-[4-(Trifluoromethyl)phenyl]-2-(3,5-dichlorophenyl)ethene is a stilbene derivative of resveratrol and a selective aryl hydrocarbon receptor agonist.
References
[1] MICHAEL S DENISON Scott R N. Activation of the aryl hydrocarbon receptor by structurally diverse exogenous and endogenous chemicals.[J]. Annual review of pharmacology and toxicology, 2003, 43: 309-334. DOI: 10.1146/annurev.pharmtox.43.100901.135828
[2] PHILIPPE DE MEDINA. Synthesis and Biological Properties of New Stilbene Derivatives of Resveratrol as New Selective Aryl Hydrocarbon Modulators[J]. Journal of Medicinal Chemistry, 2004, 48 1: 287-291. DOI: 10.1021/jm0498194
1,3-DICHLORO-5-[(1E)-2(4-TRIFLUOROMETHYLPHENYL)ETHENYL]-BENZENE Preparation Products And Raw materials
Raw materials
Preparation Products
1,3-DICHLORO-5-[(1E)-2(4-TRIFLUOROMETHYLPHENYL)ETHENYL]-BENZENE Suppliers
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