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1-[2'-fluoro(1,1'-biphenyl)-4-yl]ethan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

345-55-1

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345-55-1 Usage

Type of compound

Ketone

Structural feature

Fluorine-substituted biphenyl group

Potential applications

a. Organic synthesis
b. Pharmaceutical research

Usage

Building block in the synthesis of various organic molecules and pharmaceutical drugs

Research status

Further research needed to fully understand its potential uses and applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 345-55-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 345-55:
(5*3)+(4*4)+(3*5)+(2*5)+(1*5)=61
61 % 10 = 1
So 345-55-1 is a valid CAS Registry Number.

345-55-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(2-fluorophenyl)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names EINECS 206-461-6

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:345-55-1 SDS

345-55-1Relevant academic research and scientific papers

Lipid-lowering (hetero)aromatic tetrahydro-1,4-oxazine derivatives with antioxidant and squalene synthase inhibitory activity

Kourounakis, Angeliki P.,Charitos, Christos,Rekka, Eleni A.,Kourounakis, Panos N.

supporting information; experimental part, p. 5861 - 5865 (2009/09/25)

A number of newly synthesized 2-[4-(hetero)aromatic]phenyl-2-hydroxy- tetrahydro-1,4-oxazine derivatives were found to inhibit lipid peroxidation (IC50 of the most potent was 20 μM) as well as rat squalene synthase (IC50 for most between 1-10 μM). Antidyslipidemic action was demonstrated in vivo: the most active compound decreased triglycerides, total cholesterol, and LDL-cholesterol of hyperlipidemic rats by 64, 67, and 82%, respectively, at 56 μmol/kg (ip). Most of the novel compounds are more active than the structurally related and reference biphenyl-morpholine, pointing to useful structural approaches for the design of antiatherosclerotic agents.

Polyvinylpyridine, a versatile solid phase for coordinative immobilisation of palladium precatalysts - Applications in Suzuki-Miyaura reactions

Solodenko, Wladimir,Mennecke, Klaas,Vogt, Carla,Gruhl, Susan,Kirschning, Andreas

, p. 1873 - 1881 (2008/01/27)

The immobilisation of an oxime-based palladacycle on polyvinylpyridine (PVP) resin affords a reusable, air, moisture and thermally stable palladium precatalyst which exerts high activity in Suzuki-Miyaura reactions both in batch as well as continuous-flow processes. Evidence is presented which shows that, besides serving as an anchor for the precatalyst, PVP also acts as a scavenger for Pd particles present in solution. Georg Thieme Verlag Stuttgart.

Sulfonamide derivatives

-

, (2008/06/13)

The present invention provides certain sulfonamide derivatives useful for potentiating glutamate receptor function in a mammal and therefore, useful for treating a wide variety of conditions, such as psychiatric and neurological disorders.

Isoxazole derivatives

-

, (2008/06/13)

An isoxazole derivative represented by the formula: or a pharmaceutically acceptable salt thereof useful as a therapeutic drug for auto-immune diseases and inflammatory diseases.

Liquid Crystalline Polymesomorphism in Copper(II) Complexes of β-Diketones: The Effect of the Position of a Polar Substituent

Thompson, Neil J.,Goodby, John W.,Toyne, Kenneth J.

, p. 81 - 96 (2007/10/02)

We have shown previously that smetic phase thermal stability in copper(II) complexes of 1-(4'-decylbiphenyl-4-yl)-3-(biphenyl-4-yl)propane-1,3-diones is considerably enhanced by the introduction of polar substituents (F, Br and CF3) into the 4'-position of the lateral biphenyl unit.The preparation of a new series of complexes is described and the transition temperatures of the ligands and complexes reveal the effect on mesophase type and stability of a polar substituent at different positions in the molecule.The effects which fluoro-substituents have on the transitiontemperatures of the β-diketone ligands and the complexes are also compared with the effects produced by similar fluoro-subsitution in terphenyl systems.

Formation Constants of Cyanohydrins of Substituted Acetylbiphenyls

Ananthakrishnanadar, P.,Kannan, N.

, p. 74 - 75 (2007/10/02)

The formation constants of cyanohydrins of 2'- and 3'-substituted 4-acetylbiphenyls have been determined at 30 deg C in 80percent dioxan-water (v/v).The 3'-substituted 4-acetylbiphenyls obey the Hammett equation giving a ρ-value of 0.52; 2'-substituted cyanohydrins do not obey the Hammett equation.The formation constants of 3'-substituted 4-acetylbiphenyls and their rate constants for the reduction by sodium borohydride reveal a linear relationship (r = 0.990).The influence of 2'-substituents reveals the existence of ?-electron steric effect.

N-1-(p-Biphenylalkyl)piperazines and their use as anti-inflammatory agents

-

, (2008/06/13)

This invention relates to N-1(p-biphenylalkyl) piperazines, to the processes for making such compounds and to the use of such compounds as anti-inflammatory agents, particularly useful in the treatment of rheumatoid arthritis.

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