85017-60-3

Basic information

• Product Name: 4-IODOPENTYLBENZENE
• Synonyms: P-PENTYLIODOBENZENE;P-IODOPENTYLBENZENE;4-IODOPENTYLBENZENE;1-Iodo-4-pentylbenzene;1-Iodo-4-n-pentylbenzene
• CAS NO: 85017-60-3
• Molecular Formula: C₁₁H₁₅I
• Molecular Weight: 274.14
• Mol File: 85017-60-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 88 °C
• Flash Point: 88°C/1mm
• Appearance: /
• Density: 1,38 g/cm3
• Vapor Pressure: 0.0139mmHg at 25°C
• Refractive Index: 1.559
• Sensitive: Light Sensitive
• CAS DataBase Reference: 4-IODOPENTYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-IODOPENTYLBENZENE(85017-60-3)
• EPA Substance Registry System: 4-IODOPENTYLBENZENE(85017-60-3)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 85017-60-3(Hazardous Substances Data)

Usage

General Description

4-Iodopentylbenzene is a chemical compound with the molecular formula C12H17I. It is a derivative of benzene and contains both a benzene ring and a pentyl group with an iodine atom attached. This chemical is mainly used in organic synthesis and pharmaceutical research. It is commonly used as a starting material in the production of various pharmaceuticals and agrochemicals. 4-Iodopentylbenzene is also utilized in the synthesis of various other organic compounds, and its versatile reactivity makes it a valuable building block in the field of organic chemistry. Additionally, it has potential applications in biological and medicinal research due to its ability to modulate specific biological targets.

InChI:InChI=1/C11H15I/c1-2-3-4-5-10-6-8-11(12)9-7-10/h6-9H,2-5H2,1H3

Upstream product

• 33228-44-3 4-pentylaniline 
• 95857-32-2 1-(4-nitrophenyl)pentane 
• 17763-80-3 para-nitrophenyl triflate 
• 4737-50-2 n-pentylboronic acid 
• 591-50-4 iodobenzene 
• 638-29-9 n-valeryl chloride 

Downstream Products

• 331834-00-5 5-bromo-2-(4-pentyl-phenyl)-benzofuran 
• 121219-12-3 (4-pentylphenyl)boronic acid 
• 1359844-02-2 4,4,5,5-tetramethyl-2-(4-pentylphenyl)-1,3,2-dioxaborolane 
• 29148-31-0 diethyl (4-pentylphenyl)malonate 
• 10270-29-8 p-n-pentylbenzonitrile 
• 138220-08-3 1-(4-pentylphenyl)-2-(trimethylsilyl)acetylene 

Relevant articles and documents

Boron clusters in liquid crystals

3-Dimensional aromatic moiety was used for the first time in the synthesis of liquid crystals. Several of the prepared compounds, based on σ-aromatic boron clusters 1 and 2, show only nematic mesophases with relatively high Ti, good electrochemical but limited thermal stability. Absorption and emission spectra of pyridine derivative 15 are reported. Semiempirical methods were employed in evaluation of molecular properties and design of molecules with large coaxial dipole moments.

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.