40745-49-1

Usage

Uses

Used in Agricultural Applications:
1-Chloroacenaphthene is used as a polyploidizing agent in plants for promoting the development of polyploidy, which can lead to increased vigor, stress resistance, and improved crop yields. Its application in this field is based on its ability to induce chromosomal changes in plant cells, resulting in the formation of polyploid organisms.
Used in Environmental Applications:
1-Chloroacenaphthene is used as an indicator of air pollution due to its presence in the atmosphere as a result of incomplete combustion processes. Monitoring the levels of 1-Chloroacenaphthene can provide valuable information on the efficiency of combustion systems and the potential impact of air pollution on human health and the environment.

Upstream product

• 6306-07-6 1-acenaphthenol 
• 83-32-9 acenaphthene 
• 56-23-5 tetrachloromethane 
• 7782-50-5 chlorine 
• 2235-15-6 1(2H)-acenaphthylenone 
• 5121-00-6 naphthalen-1-yl-acetyl chloride 
• 86-87-3 naphth-1-yl acetic acid 

Downstream Products

• 1616852-94-8 C₄₂H₄₃N₃O₂ 
• 81-84-5 1,8-Naphthalic anhydride 

Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AND METHODS OF USE THEREOF

Provided herein are heterocyclyl compounds, methods of their synthesis, pharmaceutical compositions comprising the compounds, and methods of their use. The compounds provided herein are useful for the treatment, prevention, and/or management of various neurological disorders, including but not limited to, psychosis and schizophrenia.

Interpretation of retention indices in gas chromatography for establishing structures of isomeric products of alkylarenes radical chlorination

By an example of previously uncharacterized products obtained by alkylarenes radical chlorination was demonstrated that combination of various interpretation methods applied to the retention indices (RI) in the gas chromatography on the standard nonpolar phases (comparison of RI of products and initial compounds, characteristics of succession of the chromatographic elution of the structural isomers with the use of estimation of molecular dynamic parameters, application of the additive schemes to RI calculation, and using of structural analogy CH3?Cl for testing the results obtained) permitted unambiguous identification of the structure even without data of mass spectrometry.

Mild chlorination of aromatic compounds with tin(IV) chloride and lead tetraacetate

SnCl4/Pb(OAc)4 acts as a safe source of Cl2 for the chlorination of aromatic compounds. A variety of aromatic compounds are effectively chlorinated with SnCl4/Pb(OAc)4 under mild conditions. The mixture is a selective chlorinating agent, particularly with polyalkylbenzenes, polycyclic aromatic compounds and anisoles.