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2',4',5'-TRIFLUOROPROPIOPHENONE - CAS 220228-07-9

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Category
Main Product
Product Name
2',4',5'-TRIFLUOROPROPIOPHENONE
Catalog Number
220228-07-9
Synonyms
2',4',5'-TRIFLUOROPROPIOPHENONE;2,4,5-TRIFLUOROPROPIOPHENONE
CAS Number
220228-07-9
Molecular Weight
188.15
Molecular Formula
C9H7F3O
COA
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MSDS
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Canonical SMILES
CCC(=O)C1=CC(=C(C=C1F)F)F
InChI
InChI=1S/C9H7F3O/c1-2-9(13)5-3-7(11)8(12)4-6(5)10/h3-4H,2H2,1H3
InChIKey
YPCKLYKWNGEYFG-UHFFFAOYSA-N
Structure
CAS 220228-07-9 2',4',5'-TRIFLUOROPROPIOPHENONE
Specification
Purity
95%
Boiling Point
219.1ºC at 760mmHg
Density
1.253g/cm3
Reference Reading
1.A Semi-Conductive Copper-Organic Framework with Two Types of Photocatalytic Activity.
Wu ZL1,2, Wang CH3, Zhao B4, Dong J1, Lu F3, Wang WH3, Wang WC5, Wu GJ1, Cui JZ2, Cheng P1. Angew Chem Int Ed Engl. 2016 Apr 11;55(16):4938-42. doi: 10.1002/anie.201508325. Epub 2016 Jan 6.
Based on the newly designed ligand 4'-(3,5-dicarboxyphenyl)-4,2':6',4''-terpyridine (DCTP), a unique semi-conductive 3D framework {[Cu(Ι) Cu(ΙΙ) 2 (DCTP)2 ]NO3 ⋅1.5 DMF}n (1) with a narrow band gap of 2.1 eV, was obtained and structurally characterized. DFT calculations with van de Waals correction employed to explore the electronic structure of 1, clearly revealed its semi-conductive behavior. Furthermore, we found that 1 exhibits a superior band alignment with water to produce hydrogen and degrade organic pollutants. Without adding any photosensitizers, 1 displays an efficiently photocatalytic hydrogen production in water based on the photo-generated electrons under UV/Vis light. 1 also exhibits excellent photo-degradation of methyl blue under visible-light owing to the strong oxidization of excited holes. It is the first example of MOFs with doubly photocatalytic activities related to photo-generated electrons and holes, respectively.
2.Coumarins from Angelica decursiva inhibit α-glucosidase activity and protein tyrosine phosphatase 1B.
Ali MY1, Jannat S1, Jung HA2, Jeong HO3, Chung HY3, Choi JS4. Chem Biol Interact. 2016 Apr 13. pii: S0009-2797(16)30143-0. doi: 10.1016/j.cbi.2016.04.020. [Epub ahead of print]
In the present study, we investigated the anti-diabetic potential of six natural coumarins, 4-hydroxy Pd-C-III (1), 4'-methoxy Pd-C-I (2), decursinol (3), decursidin (4), umbelliferone 6-carboxylic acid (5), and 2'-isopropyl psoralene (6) isolated from Angelica decursiva and evaluated their inhibitory activities against protein tyrosine phosphatase 1B (PTP1B), α-glucosidase, and ONOO--mediated protein tyrosine nitration. Coumarins 1-6 showed potent PTP1B and α-glucosidase inhibitory activities with ranges of IC50 values of 5.39-58.90 μM and 65.29-172.10 μM, respectively. In the kinetic study for PTP1B enzyme inhibition, compounds 1, 5, and 6 were competitive, whereas 2 and 4 showed mixed type, and 3 displayed noncompetitive type inhibition. For α-glucosidase enzyme inhibition, compounds 1 and 3 exhibited good mixed-type, while 2, 5, and 6 showed noncompetitive and 4 displayed competitive type inhibition. Furthermore, these coumarins also effectively suppressed ONOO--mediated tyrosine nitration in a dose-dependent manner.
3.Dinuclear Ruthenium Complex Based on a π-Extended Bridging Ligand with Redox-Active Tetrathiafulvalene and 1,10-Phenanthroline Units.
Chen B1, Lv ZP1, Hua C2, Leong CF2, Tuna F3, D'Alessandro DM2, Collison D3, Zuo JL1. Inorg Chem. 2016 Apr 12. [Epub ahead of print]
The synthesis of a π-extended bridging ligand with both redox-active tetrathiafulvalene (TTF) and 1,10-phenanthroline (phen) units, namely, bis(1,10-phenanthro[5,6-b])tetrathiafulvalene (BPTTF), was realized via a self-coupling reaction. Using this ligand and Ru(tbbpy)2Cl2 (tbbpy = 4,4'-di-tert-butyl-2,2'-bipyridine), the dinuclear ruthenium(II) compound [{Ru(tbbpy)2}2(BPTTF)](PF6)4 (1) has been obtained by microwave-assisted synthesis. Structural characterization of 1 revealed a crossed arrangement of the TTF moieties on adjacent dimers within the crystal structure. The optical and redox properties of 1 were investigated using electrochemical, spectroelectrochemical, electron paramagnetic resonance (EPR), and absorption spectroscopic studies combined with theoretical calculations. One exhibits a rich electrochemical behavior owing to the multiple redox-active centers. Interestingly, both the ligand BPTTF and the ruthenium compound 1 are EPR-active in the solid state owing to intramolecular charge-transfer processes.
4.Paeonol enhances thrombus recanalization by inducing vascular endothelial growth factor 165 via ERK1/2 MAPK signaling pathway.
Ye S1, Liu X2, Mao B1, Yang L1, Liu N1. Mol Med Rep. 2016 Apr 15. doi: 10.3892/mmr.2016.5135. [Epub ahead of print]
Paeonol (2'-hydroxy-4'-methoxyacetophenone) is the major active compound of Mautan cortex and has been demonstrated to inhibit platelet aggregation in previous studies. The current study aimed to elucidate the underlying molecular mechanism of paeonol in recanalizing thrombi. The presence of indicators of prothrombotic state (PTS) in the serum of the model animals were determined by enzyme‑linked immunosorbent assay (ELISA) assay and the cytotoxicity of paeonol on human umbilical vein endothelial cell (HUVEC) cultures was estimated by 3‑(4,5 dimethylthiazol‑2‑yl)-2,5-diphenyltetrazolium bromide assay. The possible underlying signaling pathway involved in the interaction between paeonol and vascular endothelial growth factor 165 (VEGF165) was investigated using western blotting. The levels of 6‑keto‑prostaglandin F1α, fibronectin, and VEGF165 in serum were significantly upregulated by the treatment of paeonol while the levels of fibrinogen, D‑dimer, and thromboxane B2 were significantly downregulated (P<0.
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