131894-91-2

Usage

Uses

Used in Organic Synthesis:
1-N-Heptyl-4-iodobenzene is used as a key intermediate in the synthesis of various organic compounds, contributing to the formation of complex molecules and structures.
Used in Pharmaceutical Production:
1-N-Heptyl-4-iodobenzene is utilized as a building block in the production of pharmaceuticals, playing a crucial role in the development of new drugs and medications.
Used in Agrochemical Production:
1-N-HEPTYL-4-IODOBENZENE is also used in the creation of agrochemicals, which are essential for enhancing crop protection and agricultural productivity.
Used in Fine Chemicals Production:
1-N-Heptyl-4-iodobenzene is employed in the synthesis of fine chemicals, which are high-purity chemicals used in various industries, including cosmetics, fragrances, and specialty chemicals.
Used as a Research and Laboratory Reagent:
In research and laboratory settings, 1-N-Heptyl-4-iodobenzene serves as a reagent for conducting experiments and exploring new chemical reactions and processes. Its unique structure and properties make it a valuable tool for scientific investigation.

InChI:InChI=1/C13H19I/c1-2-3-4-5-6-7-12-8-10-13(14)11-9-12/h8-11H,2-7H2,1H3

Upstream product

• 50606-96-7 4-heptylbenzoyl chloride 
• 17763-80-3 para-nitrophenyl triflate 
• 28741-07-3 heptyl boronic acid 
• 62-53-3 aniline 
• 111-70-6 n-heptan1ol 
• 37529-27-4 4-heptylaniline 

Downstream Products

• 913653-77-7 2-(4-heptylphenyl)-1,3-propanediol 
• 256383-44-5 4-(n-heptyl)phenylboronic acid 
• 1359844-04-4 4-heptylphenylboronic acid pinacol ester 
• 743437-79-8 1-heptyl-4-(trifluoromethyl)benzene 
• 39969-30-7 1,2-bis(4-heptylphenyl)ethyne 
• 57045-20-2 p-Heptylzimtsaeure 
• 1374220-23-1 C₁₈H₂₈Si 

Relevant academic research and scientific papers

REACTIVE PERPENDICULAR ALIGNED MATERIAL, LIQUID CRYSTAL DISPLAY PANEL, AND METHOD OF LIQUID CRYSTAL ALIGNMENT

The disclosure provides a reactive perpendicular aligned material, a liquid crystal display panel, and a method for aligning liquid crystals, a general structural formula of the reactive perpendicular aligned material is A-Z—R, A is —CH═CH—COOH; Z is wher

Metathesis-active ligands enable a catalytic functional group metathesis between aroyl chlorides and aryl iodides

Current methods for functional group interconversion have, for the most part, relied on relatively strong driving forces which often require highly reactive reagents to generate irreversibly a desired product in high yield and selectivity. These approaches generally prevent the use of the same catalytic strategy to perform the reverse reaction. Here we describe a catalytic functional group metathesis approach to interconvert, under CO-free conditions, two synthetically important classes of electrophiles that are often employed in the preparation of pharmaceuticals and agrochemicals—aroyl chlorides (ArCOCl) and aryl iodides (ArI). Our reaction design relies on the implementation of a key reversible ligand C–P bond cleavage event, which enables a non-innocent, metathesis-active phosphine ligand to mediate a rapid aryl group transfer between the two different electrophiles. Beyond enabling a practical and safer approach to the interconversion of ArCOCl and ArI, this type of ligand non-innocence provides a blueprint for the development of a broad range of functional group metathesis reactions employing synthetically relevant aryl electrophiles.

Design and synthesis of boronic acid inhibitors of endothelial lipase

Endothelial lipase (EL) and lipoprotein lipase (LPL) are homologous lipases that act on plasma lipoproteins. EL is predominantly a phospholipase and appears to be a key regulator of plasma HDL-C. LPL is mainly a triglyceride lipase regulating (V)LDL levels. The existing biological data indicate that inhibitors selective for EL over LPL should have anti-atherogenic activity, mainly through increasing plasma HDL-C levels. We report here the synthesis of alkyl, aryl, or acyl-substituted phenylboronic acids that inhibit EL. Many of the inhibitors evaluated proved to be nearly equally potent against both EL and LPL, but several exhibited moderate to good selectivity for EL.