Welcome to LookChem.com Sign In|Join Free
  • or
2-bromo-1-(4-chloro-2-fluorophenyl)ethanone is a chemical compound that features a benzene ring with a 4-chloro-2-fluoro substitution, a carbonyl group, and a two-carbon chain with a bromine atom attached to one of the carbons. 2-bromo-1-(4-chloro-2-fluorophenyl)ethanone is known for its structural properties and reactivity, making it a valuable component in various chemical processes.

725743-41-9

Post Buying Request

725743-41-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

725743-41-9 Usage

Uses

Used in Pharmaceutical Synthesis:
2-bromo-1-(4-chloro-2-fluorophenyl)ethanone is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agrochemical Production:
2-bromo-1-(4-chloro-2-fluorophenyl)ethanone also serves as an intermediate in the production of agrochemicals, playing a role in the creation of substances used in agriculture to protect crops and enhance yields.
Used in Organic Compound Production:
2-bromo-1-(4-chloro-2-fluorophenyl)ethanone is employed in the synthesis of various organic compounds, which are essential for a wide range of applications across different industries.
Used in Material Development:
Due to its unique structure and reactivity, 2-bromo-1-(4-chloro-2-fluorophenyl)ethanone is used in the development of new materials, potentially leading to advancements in various fields.
Used in Medicinal Chemistry:
2-bromo-1-(4-chloro-2-fluorophenyl)ethanone has potential applications in medicinal chemistry, where its properties can be leveraged to create innovative and effective treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 725743-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,5,7,4 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 725743-41:
(8*7)+(7*2)+(6*5)+(5*7)+(4*4)+(3*3)+(2*4)+(1*1)=169
169 % 10 = 9
So 725743-41-9 is a valid CAS Registry Number.

725743-41-9Relevant academic research and scientific papers

HETEROCYCLIC GLP-1 AGONISTS

-

Page/Page column 177-178; 114-115, (2021/11/06)

This disclosure relates to GLP-1 agonists of Formula (I): including pharmaceutically acceptable salts and solvates thereof, and pharmaceutical compositions including the same.

Synthetic method of pibrentasvir intermediate

-

Paragraph 0036-0039, (2019/04/30)

The invention relates to the technical field of organic synthesis, in particular to a synthetic method of a pibrentasvir intermediate. The synthetic method comprises the steps that S1, a compound IV and a bromination reagent are subjected to a bromination

COMPOSITIONS AND METHODS FOR CONTROL OF DISEASE

-

Paragraph 0311; 0319, (2018/08/30)

Compounds, compositions and methods for controlling root-originating diseases are described herein. The compounds include oxazoles, oxadiazoles and thiadiazoles. The compounds may be administered to plants, seeds, and/or soil.

COMPOSITIONS AND METHODS FOR IMPROVING AGRONOMIC CHARACTERISTICS OF PLANTS

-

Paragraph 0399, (2016/07/05)

Compounds, compositions and methods for improving one or more agronomic characteristics of desired crop plants are described herein. The compounds include oxazoles, oxadiazoles and thiadiazoles.

Compostions and Methods for Controlling Nematodes

-

Page/Page column 39, (2009/03/07)

Compositions and processes for controlling nematodes are described herein, e.g., nematodes that infest plants or animals. The compounds include oxazoles, oxadiazoles and thiadiazoles.

Process for producing optically active carbinols

-

, (2008/06/13)

The present invention relates to a process for producing optically active halomethyl phenyl carbinols of the formula (1), comprising reducing halomethyl phenyl ketones of the formula (2) using an asymmetric reducing agent obtained from boranes and optically active α-phenyl-substituted-β-amino alcohols of the formula (3) or optically active α-non-substituted-β-amino alcohols of the formula (4). The present invention further relates to a process for producing optically active carbinols, comprising reacting a prochiral keytone with an asymmetric reducing agent obtained from optically active β-amino alcohols of the formula (5), a metal boron hydride and Lewis acid or lower dialkyl sulfuric acid. All of the formulas (1) to (5) are the same as shown in the specification.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 725743-41-9