95306-89-1

Basic information

• Product Name: 1-IODO-4-PROPOXYBENZENE
• Synonyms: 1-IODO-4-PROPOXYBENZENE
• CAS NO: 95306-89-1
• Molecular Formula: C₉H₁₁IO
• Molecular Weight: 262.0875
• Mol File: 95306-89-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 268.2 °C at 760 mmHg
• Flash Point: 116 °C
• Appearance: /
• Density: 1.555g/cm³
• CAS DataBase Reference: 1-IODO-4-PROPOXYBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-IODO-4-PROPOXYBENZENE(95306-89-1)
• EPA Substance Registry System: 1-IODO-4-PROPOXYBENZENE(95306-89-1)

Safety Data

• Hazardous Substances Data: 95306-89-1(Hazardous Substances Data)

Usage

Description

1-IODO-4-PROPOXYBENZENE is a chemical compound with the molecular formula C9H11IO, characterized by a benzene ring with a propoxy (C3H7O) group and an iodo (I) substituent attached at the 1-position. It is an aromatic halide, known for its clear, colorless to pale yellow liquid form with a faint odor. Due to its flammability and potential harmfulness, it requires careful handling and storage.

Uses

Used in Organic Synthesis:
1-IODO-4-PROPOXYBENZENE is used as a key intermediate in organic synthesis for the production of various compounds, leveraging its aromatic halide properties to facilitate chemical reactions.
Used in Pharmaceutical Industry:
1-IODO-4-PROPOXYBENZENE is used as a starting material for the synthesis of pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Industry:
1-IODO-4-PROPOXYBENZENE is used as a precursor in the synthesis of agrochemicals, playing a role in the creation of pesticides and other agricultural products.
Used in Liquid Crystal Production:
1-IODO-4-PROPOXYBENZENE is used in the production of liquid crystals, which are essential components in display technologies and other applications requiring responsive molecular materials.
Used in Functional Materials:
1-IODO-4-PROPOXYBENZENE is utilized in the development of functional materials, where its unique chemical structure imparts specific properties useful in various high-tech applications.

Upstream product

• 540-54-5 1-Chloropropane 
• 540-38-5 p-Iodophenol 
• 107-08-4 1-iodo-propane 
• 106-94-5 propyl bromide 

Downstream Products

• 116223-45-1 4-[(E)-2-(4-Propoxy-phenyl)-vinyl]-pyridine 
• 39604-97-2 4-n-propyloxyphenylacetylene 
• 29148-19-4 diethyl (4-propoxyphenyl)malonate 
• 913653-73-3 2-(4-propoxyphenyl)-1,3-propanediol 
• 1352545-30-2 1-(3,4,5-trimethoxyphenyl)-5-(4-propoxyphenyl)-1H-tetrazole 
• 469859-73-2 1-propoxy-4-[2-(trimethylsilyl)ethynyl]benzene 

Relevant articles and documents

Organic hole transport material and preparation method and application thereof

The invention provides an organic hole transport material and a preparation method and application thereof. The structural general formula of the organic hole transport material is shown in the specification, and in the formula, R is ethyl, propyl, isopropyl or butyl. The preparation method is simple and easy to implement, the structure is definite, and the prepared organic hole transport materialhas high photoelectric conversion efficiency and can be applied to perovskite solar cells.

Macrocyclic inhibitors of the PD-1/PD-L1 and CD80(B7-1)/PD-L1 protein/protein interactions

The present disclosure provides novel macrocyclic peptides which inhibit the PD-1/PD-L1 and PD-L1/CD80 protein/protein interaction, and thus are useful for the amelioration of various diseases, including cancer and infectious diseases.

Synthesis of diphenyl-diacetylene-based nematic liquid crystals and their high birefringence properties

We synthesized two series of diphenyl-diacetylene (DPDA)-based materials with alkoxy and alkyl tails of length m (DPDA-OCm and DPDA-Cm, respectively), and measured their nematic-phase birefringence (Δn) as a function of wavelength and temperature. We found that Δn decreases with an increase in m, possibly by a dilution effect of the low-Δn alkyl tail. Further, of the two series, Δn was found to be relatively higher in the DPDA-OCm materials, with the highest value of 0.4 obtained for DPDA-OC1 at 550 nm at 10 °C below the isotropic-to-nematic transition temperature. Further, we observed the temperature dependence for Δn, which is proportional to the order parameter (s). From extrapolation to s = 1 (the perfect orientation state), it is speculated that the DPDA-O moiety has the potential to afford a very large Δn of 0.9. The Royal Society of Chemistry 2012.