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19672-61-8

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19672-61-8 Usage

Description

4-BROMO-4'-CHLOROCHALCONE is a chemical compound belonging to the class of chalcones, characterized as a yellow solid with a molecular formula of C15H9BrClO and a molecular weight of 311.59 g/mol. It is recognized for its potential as an antibacterial, antifungal, anti-inflammatory, and anti-cancer agent, and is utilized as a building block in organic synthesis for creating various biologically active compounds.

Uses

Used in Pharmaceutical Industry:
4-BROMO-4'-CHLOROCHALCONE is used as an antibacterial and antifungal agent for its demonstrated activity against a range of pathogens, making it a promising candidate for the development of new pharmaceuticals.
Used in Anti-inflammatory Applications:
4-BROMO-4'-CHLOROCHALCONE is used as an anti-inflammatory agent, leveraging its potential to reduce inflammation and alleviate related symptoms.
Used in Anti-cancer Applications:
4-BROMO-4'-CHLOROCHALCONE is used as an anti-cancer agent, showing promise in the development of new pharmaceuticals for cancer treatment.
Used in Organic Synthesis:
4-BROMO-4'-CHLOROCHALCONE is used as a building block in organic synthesis for the preparation of various biologically active compounds, contributing to the advancement of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 19672-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,7 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19672-61:
(7*1)+(6*9)+(5*6)+(4*7)+(3*2)+(2*6)+(1*1)=138
138 % 10 = 8
So 19672-61-8 is a valid CAS Registry Number.

19672-61-8SDS

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 4-BROMO-4'-CHLOROCHALCONE

1.2 Other means of identification

Product number -
Other names 4'-bromo-4-chloro-2,6-difluorobiphenyl

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:19672-61-8 SDS

19672-61-8Relevant articles and documents

Catalyst- and acid-free Markovnikov hydration of alkynes in a sustainable H2O/ethyl lactate system

Dandia, Anshu,Saini, Pratibha,Chithra,Vennapusa, Sivaranjana Reddy,Parewa, Vijay

, (2021/03/15)

An efficient and sustainable protocol for the hydration of alkynes has been developed under metal/acid/catalyst/ligand-free conditions in a water/ethyl lactate mixture. The hydrogen-bond network in the ethyl lactate and water mixture plays a crucial and decisive role in activating the alkynes for hydration to afford the corresponding methyl ketones. This strategy gives the Markovnikov (ketone) addition product selectively over other possible products. The essential role of hydrogen bonding has been confirmed by experimental and theoretical techniques. A probable mechanism has been suggested by various control tests. The efficacy of the method has been further explored for the competent production of value-added α,β-unsaturated carbonyl compounds through the reaction of aldehydes with alkynes as ketonic surrogates. The environmentally benign hydration method takes place under mild conditions, has broad functional-group compatibility, and uses the ethyl lactate/water (1:3) medium as a “green alternative” in the absence of any hazardous, harmful, or expensive substances.

Environment Friendly Synthesis of N′-(1,3-Diphenylallylidene)-1-ethyl-7-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carbohydrazides: Crystal Structure and Their Anti-oxidant Potential

Mubarak, Shafaq,Zia-Ur-Rehman, Muhammad,Jamil, Nadia,Zaheer, Muhammad,Arshad, Muhammad Nadeem,Asiri, Abdullah Mohammad

, p. 1191 - 1200 (2019/11/19)

An environment friendly synthesis of novel hybrid pharmacophores derived from synergism of nalidixic acid and 1,3-diphenylprop-2-en-1-ones is described. Percent yield and reaction times of microwave assisted reactions have been compared with the reactions

Monoamine Oxidase Inhibitory Activity: Methyl- versus Chlorochalcone Derivatives

Mathew, Bijo,U?ar, Gülberk,Mathew, Githa Elizabeth,Mathew, Sincy,Kalatharakkal Purapurath, Praseedha,Moolayil, Fasil,Mohan, Smrithy,Varghese Gupta, Sheeba

, p. 2649 - 2655 (2016/12/23)

Numerous studies have shown that chalcones are promising scaffolds for the development of new monoamine oxidase-B (MAO-B) inhibitors. As a continuation of our ongoing research into the development of reversible human MAO-B (hMAO-B) inhibitors, two series

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