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54916-27-7

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54916-27-7 Usage

General Description

1-(4-(4-Bromophenoxy)phenyl)ethanone is a chemical compound that belongs to the family of ketones. It is a white crystalline solid with the molecular formula C16H13BrO2 and a molecular weight of 315.18 g/mol. 1-(4-(4-BROMOPHENOXY)PHENYL)ETHANONE is used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active compounds. It is a versatile and important intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. The bromine atom in its structure makes it a versatile compound for further derivatization and modification, allowing for the development of new drugs and chemical compounds through synthetic pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 54916-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,1 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54916-27:
(7*5)+(6*4)+(5*9)+(4*1)+(3*6)+(2*2)+(1*7)=137
137 % 10 = 7
So 54916-27-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H11BrO2/c1-10(16)11-2-6-13(7-3-11)17-14-8-4-12(15)5-9-14/h2-9H,1H3

54916-27-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-(4-Bromophenoxy)Phenyl)Ethanone

1.2 Other means of identification

Product number -
Other names 1-[4-(4-bromophenoxy)phenyl]ethanone

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:54916-27-7 SDS

54916-27-7Relevant articles and documents

Exploring Tandem Ruthenium-Catalyzed Hydrogen Transfer and SNAr Chemistry

Polidano, Kurt,Reed-Berendt, Benjamin G.,Basset, Ana?s,Watson, Andrew J. A.,Williams, Jonathan M. J.,Morrill, Louis C.

, p. 6716 - 6719 (2017/12/26)

A hydrogen-transfer strategy for the catalytic functionalization of benzylic alcohols via electronic arene activation, accessing a diverse range of bespoke diaryl ethers and aryl amines in excellent isolated yields (38 examples, 70% average yield), is reported. Taking advantage of the hydrogen-transfer approach, the oxidation level of the functionalized products can be selected by judicious choice of simple and inexpensive additives.

Ligand-free copper-catalyzed O-arylation of nitroarenes with phenols

Chen, Jiuxi,Wang, Xingyong,Zheng, Xingwang,Ding, Jinchang,Liu, Miaochang,Wu, Huayue

supporting information, p. 8905 - 8907 (2012/10/29)

The first example of ligand-free copper-catalyzed O-arylation of nitroarenes with phenols was developed, achieving unsymmetrical diaryl ethers in moderate to excellent yields. This arylation proceeded smoothly without promotion of the ligands, and displayed great functional group compatibility. Thus, the method represents a new, facile, and cost-effective approach to access unsymmetrical diaryl ethers.

Amino-pyridines as inhibitors of beta-secretase

-

Page/Page column 22, (2008/06/13)

The present invention provides an amino-pyridine compound of formula I The present invention also provides methods for the use thereof to inhibit β-secretase (BACE) and treat β-amyloid deposits and neurofibrillary tangles.

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