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40396-54-1

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40396-54-1 Usage

Description

Ethanedione, (3-bromophenyl)phenyl-, also known as 3-bromobenzoylacetylacetone, is a chemical compound with the molecular formula C14H11BrO2. It is a derivative of acetylacetone and is commonly used as a chelating ligand in coordination chemistry. Known for its ability to form stable complexes with metal ions, this versatile compound has a wide range of uses in the field of chemistry and beyond, including potential applications in pharmaceuticals and agrochemicals.

Uses

Used in Coordination Chemistry:
Ethanedione, (3-bromophenyl)phenylis used as a chelating ligand for forming stable complexes with metal ions, which is crucial in various chemical and biological applications.
Used in Organic Synthesis:
In the field of organic synthesis, ethanedione, (3-bromophenyl)phenylserves as a valuable reagent, contributing to the creation of a multitude of organic compounds.
Used in Pharmaceutical Production:
Ethanedione, (3-bromophenyl)phenylis utilized as a building block in the production of pharmaceuticals, playing a key role in the development of new drugs.
Used in Agrochemical Production:
Ethanedione, (3-bromophenyl)phenylalso finds use in the production of agrochemicals, where it may contribute to the development of more effective and targeted products for agricultural use.
Used in Anti-Cancer Research:
Ethanedione, (3-bromophenyl)phenylhas been studied for its potential anti-cancer properties, indicating its possible use in the development of cancer treatments.
Used in Anti-Inflammatory Research:
Additionally, this compound has been investigated for its anti-inflammatory properties, suggesting a potential role in the creation of treatments for inflammatory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 40396-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40396-54:
(7*4)+(6*0)+(5*3)+(4*9)+(3*6)+(2*5)+(1*4)=111
111 % 10 = 1
So 40396-54-1 is a valid CAS Registry Number.

40396-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-bromophenyl)-2-phenylethane-1,2-dione

1.2 Other means of identification

Product number -
Other names Ethanedione,(3-bromophenyl)phenyl

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:40396-54-1 SDS

40396-54-1Relevant articles and documents

Conversion of alkynes into 1,2-diketones using HFIP as sacrificial hydrogen donor and DMSO as dihydroxylating agent

Gujjarappa, Raghuram,Vodnala, Nagaraju,Putta,Ganga Reddy, Velma,Malakar, Chandi C.

supporting information, (2020/01/21)

A metal-free and hypervalent iodine free conversion of internal alkynes into 1,2-diketo compounds has been described. The efficacy of the present protocol rely on the use of HFIP (1,1,1,3,3,3-Hexafluoro-2-propanol) as reducing agent of alkynes and DMSO as dihydroxylating agent of olefins to acquire the desired chemical transformations. The obtained 1,2-diketones were further transformed into useful derivatives.

Tailoring the Molecular Properties with Isomerism Effect of AIEgens

Chen, Ming,Liu, Junkai,Liu, Feng,Nie, Han,Zeng, Jiajie,Lin, Gengwei,Qin, Anjun,Tu, Mei,He, Zikai,Sung, Herman H. Y.,Williams, Ian D.,Lam, Jacky W. Y.,Tang, Ben Zhong

, (2019/08/01)

It is challenging to achieve precise control on the properties of organic π-functional materials to widen their practical applications. On the other hand, the study of aggregation-induced emission luminogens (AIEgens) helps achieve such goals because of i

Polymer precursor and its manufacturing method for production of nano-ribbon graphene

-

Paragraph 0054; 0082-0084, (2017/01/02)

An oligophenylene monomer of general formula (I) wherein R1 and R2 are independently of each other H, halogene, —OH, —NH2, —CN, —NO2 or a linear or branched, saturated or unsaturated C1-C40 hydrocarbon residue, which can be substituted 1- to 5-fold with h

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