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3-Bromo-5-(3-chlorophenoxy)pyridine is an organic chemical compound characterized by the presence of both bromine and chlorine atoms. It belongs to the class of aromatic halogen compounds, which are known for containing a halogen atom and a phenyl or benzene ring. As an organobromine and organochlorine compound, it is primarily utilized in synthetic chemistry as a key intermediate for the production of other chemicals. The specific applications of 3-Bromo-5-(3-chlorophenoxy)pyridine are largely dependent on the synthesis strategies employed by manufacturers. However, there is limited information available regarding its hazardousness, safety precautions, or environmental impact, indicating that it may not be extensively used or well-studied in various industries.

28232-65-7

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28232-65-7 Usage

Uses

Used in Synthetic Chemistry:
3-Bromo-5-(3-chlorophenoxy)pyridine is used as a key intermediate in the synthesis of other chemicals. Its unique structure, containing both bromine and chlorine atoms, makes it a valuable component in the production of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Bromo-5-(3-chlorophenoxy)pyridine may be used as a building block for the development of new drugs. Its specific role in drug synthesis would depend on the target molecule and the synthesis strategies employed by researchers and manufacturers.
Used in Agrochemical Industry:
3-Bromo-5-(3-chlorophenoxy)pyridine could potentially be used in the agrochemical industry for the synthesis of pesticides or other agricultural chemicals. Its application in this field would be determined by its compatibility with other chemical components and its effectiveness in addressing specific agricultural needs.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 3-Bromo-5-(3-chlorophenoxy)pyridine may be employed as a precursor for the synthesis of various dyes and pigments. Its unique structure could contribute to the development of new colorants with specific properties, such as improved stability or enhanced color intensity.
Used in Research and Development:
3-Bromo-5-(3-chlorophenoxy)pyridine can be utilized in research and development settings to explore its potential applications and properties. Scientists and researchers may investigate its reactivity, stability, and interactions with other compounds to uncover new uses and opportunities for this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 28232-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,3 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28232-65:
(7*2)+(6*8)+(5*2)+(4*3)+(3*2)+(2*6)+(1*5)=107
107 % 10 = 7
So 28232-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H7BrClNO/c12-8-4-11(7-14-6-8)15-10-3-1-2-9(13)5-10/h1-7H

28232-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-5-(3-chlorophenoxy)pyridine

1.2 Other means of identification

Product number -
Other names -

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:28232-65-7 SDS

28232-65-7Downstream Products

28232-65-7Relevant academic research and scientific papers

MTA-Cooperative PRMT5 Inhibitors

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Paragraph 0265-0268, (2021/03/19)

The present invention relates to compounds that inhibit Protein Arginine N-Methyl Transferase 5 (PRMT5) activity. In particular, the present invention relates to compounds, pharmaceutical compositions and methods of use, such as methods of treating cancer using the compounds and pharmaceutical compositions of the present invention.

Structure-activity studies of 7-heteroaryl-3-azabicyclo[3.3.1]non-6-enes: A novel class of highly potent nicotinic receptor ligands

Breining, Scott R.,Melvin, Matt,Bhatti, Balwinder S.,Byrd, Gary D.,Kiser, Melanie N.,Hepler, Christopher D.,Hooker, Dawn N.,Zhang, Jenny,Reynolds, Leslie A.,Benson, Lisa R.,Fedorov, Nikolai B.,Sidach, Serguei S.,Mitchener, J. Pike,Lucero, Linda M.,Lukas, Ronald J.,Whiteaker, Paul,Yohannes, Daniel

, p. 9929 - 9945 (2013/01/16)

The potential for nicotinic ligands with affinity for the α4β2 or α7 subtypes to treat such diverse diseases as nicotine addiction, neuropathic pain, and neurodegenerative and cognitive disorders has been exhibited clinically for several compounds while p

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