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1-(4-bromophenyl)butan-2-one is an organic compound and a ketone with the chemical formula C10H11BrO. It consists of a butan-2-one (or ethylmethylketone) group attached to a phenyl ring substituted with a bromine atom at the 4-position. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. It is also used in the production of fragrances and flavoring agents. 1-(4-bromophenyl)butan-2-one is a clear, colorless liquid with a strong, sweet, and fruity odor.

200064-98-8

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200064-98-8 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-bromophenyl)butan-2-one is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into various drug molecules, contributing to the development of new medications.
Used in Organic Compounds Synthesis:
1-(4-bromophenyl)butan-2-one is used as a building block in the synthesis of other organic compounds, facilitating the creation of a wide range of chemical products.
Used in Fragrance Industry:
1-(4-bromophenyl)butan-2-one is used as a component in the production of fragrances for its strong, sweet, and fruity odor, enhancing the scent profiles of various perfumes and scented products.
Used in Flavoring Agents Industry:
1-(4-bromophenyl)butan-2-one is used in the production of flavoring agents, leveraging its distinctive fruity aroma to improve the taste and smell of food products and beverages.
It is important to handle this chemical with care, as it can be irritant to the skin, eyes, and respiratory system and should be used in a well-ventilated area with proper personal protective equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 200064-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,0,6 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 200064-98:
(8*2)+(7*0)+(6*0)+(5*0)+(4*6)+(3*4)+(2*9)+(1*8)=78
78 % 10 = 8
So 200064-98-8 is a valid CAS Registry Number.

200064-98-8Downstream Products

200064-98-8Relevant academic research and scientific papers

ANTIMICROBIAL COMPOUNDS AND METHODS

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Paragraph 00448; 00449; 00660, (2020/07/31)

The invention is directed to compounds that are active as antibacterial agents. The invention compounds are active against gram-positive and gram-negative bacteria and can be used to treat infections caused by gram-positive and gram-negative bacteria. Also disclosed are processes and intermediates for making the compounds.

Synthesis and serotonin transporter activity of sulphur-substituted α-alkyl phenethylamines as a new class of anticancer agents

Cloonan, Suzanne M.,Keating, John J.,Butler, Stephen G.,Knox, Andrew J.S.,Jorgensen, Anne M.,Peters, Guenther H.,Rai, Dilip,Corrigan, Desmond,Lloyd, David G.,Williams, D. Clive,Meegan, Mary J.

scheme or table, p. 4862 - 4888 (2010/01/16)

The discovery that some serotonin reuptake transporter (SERT) ligands have the potential to act as pro-apoptotic agents in the treatment of cancer adds greatly to their diverse pharmacological application. 4-Methylthioamphetamine (MTA) is a selective ligand for SERT over other monoamine transporters. In this study, a novel library of structurally diverse 4-MTA analogues were synthesised with or without N-alkyl and/or C-α methyl or ethyl groups so that their potential SERT-dependent antiproliferative activity could be assessed. Many of the compounds displayed SERT-binding activity as well as cytotoxic activity. While there was no direct correlation between these two effects, a number of derivatives displayed anti-tumour effects in lymphoma, leukaemia and breast cancer cell lines, showing further potential to be developed as possible chemotherapeutic agents.

New Odorless Protocols for the Synthesis of Aldehydes and Ketones from Thiol Esters

Miyazaki, Tohru,Han-Ya, Yuki,Tokuyama, Hidetoshi,Fukuyama, Tohru

, p. 477 - 480 (2007/10/03)

Dodecanethiol esters derived from odorless dodecanethiol proved to be suitable substrates for Pd-catalyzed reduction with triethylsilane, coupling with organozinc reagents, and coupling with terminal acetylenes.

A novel ketone synthesis by a palladium-catalyzed reaction of thiol esters and organozinc reagents

Tokuyama, Hidetoshi,Yokoshima, Satoshi,Yamashita, Tohru,Fukuyama, Tohru

, p. 3189 - 3192 (2007/10/03)

A variety of ketones have been prepared by a palladium-catalyzed reaction of ethanethiol esters with organozinc reagents. Various functional groups, including esters, ketones, aromatic halides and aldehydes, tolerate the reaction conditions. The reaction can also be applied to the synthesis of α-amino ketones using the corresponding L-α-amino thiol esters without racemization.

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