7048-98-8

Usage

Complex organic molecule

The compound is a complex organic molecule with a variety of functional groups and structural elements.

Thiazole ring

The compound contains a thiazole ring, which is a five-membered ring with two nitrogen atoms and one sulfur atom.

Dimethylaminoethyl group

The compound has a dimethylaminoethyl group, which is an alkyl chain with an amino group that is substituted with two methyl groups.

Propoxyphenyl group

The compound also contains a propoxyphenyl group, which is a phenyl group that is substituted with a propoxy group.

Hydroxy and carbonyl groups

The compound has a hydroxy group (-OH) and a carbonyl group (C=O), which are important functional groups in organic chemistry.

Potential applications in the pharmaceutical industry

Due to its structural features, the compound may have potential applications in the pharmaceutical industry.

Structural features contributing to pharmacological properties

The compound's structure suggests that it may have biological activity and could be of interest for further research and development.

Synthesis and characterization

The synthesis and characterization of the compound are important for understanding its potential uses and properties.

Biological activity

The compound's structure suggests that it may have biological activity, which could be explored for potential therapeutic applications.

Further research and development

The compound's potential uses and properties warrant further research and development to fully understand its capabilities and potential applications.

Upstream product

• 7097-33-8 Bicyclo<8.3.1>tetradecadien-<1(14),10,12>-diin-(4,6) 
• 85-44-9 phthalic anhydride 
• 4685-74-9 <8>paracyclophane 
• 629-03-8 1 ,6-dibromohexane 
• 108-38-3 m-xylene 
• 45037-87-4 1,8-octanediyldimagnesium dibromide 
• 541-73-1 1,3-Dichlorobenzene 
• 5297-49-4 <8>Paracyclophan-3,6-dion 
• 626-15-3 1,3-bis-(bromomethyl)benzene 
• 93807-00-2 1,3-Bis--benzol 
• 108-36-1 1,3-dibromobenzene 
• 131213-77-9 12,13-dibromo[2]metacyclo[2](2,5)thiophenophane 

Relevant academic research and scientific papers

Synthesis of [n]- and [n.n]Cyclophanes by using Suzuki-Miyaura coupling

Reaction of the bis-9-BBN adduct of several dienes with 1,3-dibromobenzene via Suzuki coupling leads to a series of [n]metacyclophanes ranging in size from 10 to 17 atom members. In each case, two carbon-carbon bonds are formed in one reaction vessel. However, when the bis-9-BBN adduct of 1,5-hexadiene is coupled with a variety of aryl dihalides, larger [n.n]cyclophanes were formed in preference to the [n]cyclophanes. Four carbon-carbon bonds are formed in this instance. Single-crystal X-ray analyses of these [n.n]cyclophanes reveal interestingly shaped molecules with large cavities.

Synthesis and Dynamic Behaviour of - and Metacyclophanes

The synthesis and structure of - and metacyclophanes 2, 4 are described.The reductive ring opening of the thiophene rings of metacyclo(2,4)- and -(2,5)thiophenophanes 1 and 3 by Raney-Ni affords the corresponding - and metacyclophanes 2

Cyclophanes, XXI. The Chemical Behavior of Paracyclophane: Reactions of the Benzene Ring

Preparative quantities of paracyclophane (1b) may be prepared from paracyclophane-3,6-dione (9) by Wolff-Kishner reduction.After a detailed dicussion of the 1H and 13C NMR spectra of 1b, its behavior in substitution and addition reactions is describ

Arenes Disubstituted with Primary Alkyl Groups from Xylylene Dianions

Xylenes were converted into dianions 1.Reaction of dianions 1 with dialkyl sulfates gave symmetrical dialkylbenzenes 2 (R = R'), while methyl iodide caused oxidative coupling followed by alkylation to give 8.Unsymmetrical dialkylbenzenes 2 (R =/= R') were made by an indirect route involving monoanions 9 and 11.Reactions of dianions 1 with dihalides gave cyclophanes o-3 (n = 5,6,9), m-3 (n = 8-10), and p-3 (n = 9-11) and cyclophanes o-4 (n = 2,5,7,9) and m-4 (n = 2,6,7).Dianion 5 from 2,6-lutidine was used to prepare nitrogen analogues of 2 (R = R') and m-3 (n = 8-10).