54609-15-3

Usage

Uses

Used in Pharmaceutical Production:
2,4-Dimethyl-1H-pyrrole-1-propan-1-ol is used as an intermediate in the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds due to its reactive chemical properties.
Used in Pesticide Synthesis:
In the agricultural sector, 2,4-Dimethyl-1H-pyrrole-1-propan-1-ol is utilized as an intermediate in the synthesis of pesticides, playing a role in developing effective crop protection agents.
Used in Organic Compounds Synthesis:
2,4-Dimethyl-1H-pyrrole-1-propan-1-ol is also used as an intermediate in the synthesis of other organic compounds, showcasing its versatility in chemical reactions and its ability to form a wide range of products.
Used in Fragrance and Flavor Industry:
2,4-Dimethyl-1H-pyrrole-1-propan-1-ol is used as a building block in the synthesis of fragrance and flavor ingredients, capitalizing on its pleasant odor to enhance consumer products.
Used in Organic Electronics:
With its unique molecular structure, 2,4-Dimethyl-1H-pyrrole-1-propan-1-ol has potential applications in the field of organic electronics, where it may contribute to the development of novel electronic materials and devices.
Used in Material Science:
2,4-Dimethyl-1H-pyrrole-1-propan-1-ol's properties also make it suitable for applications in material science, where it could be employed in the creation of new materials with specific characteristics for various uses.

Upstream product

• 2935-44-6 hexane-2,5-diol 
• 156-87-6 propan-1-ol-3-amine 
• 110-13-4 2,5-hexanedione 

Downstream Products

• 101778-57-8 3-cyclohexyl-propionic acid-[3-(2,5-dimethyl-pyrrol-1-yl)-propyl ester] 
• 102455-98-1 5-phenyl-valeric acid-[3-(2,5-dimethyl-pyrrol-1-yl)-propyl ester] 
• 102456-63-3 4-cyclohexyl-hexanoic acid-[3-(2,5-dimethyl-pyrrol-1-yl)-propyl ester] 

Relevant academic research and scientific papers

Sustainable Manganese-Catalyzed Solvent-Free Synthesis of Pyrroles from 1,4-Diols and Primary Amines

A general and selective metal-catalyzed conversion of biomass-derived primary diols and amines to the highly valuable 2,5-unsubstituted pyrroles has been developed. The reaction is catalyzed by a stable nonprecious manganese complex (1 mol %) in the absence of organic solvents whereby water and molecular hydrogen are the only side products. The manganese catalyst shows unprecedented selectivity, avoiding the formation of pyrrolidines, cyclic imides, and lactones.

An easy synthetic way to exfoliate and stabilize MWCNTs in a thermoplastic pyrrole-containing matrix assisted by hydrogen bonds

This work focuses on the design of an engineered thermoplastic polymer containing pyrrole units in the main chain and hydroxyl pendant groups (A-PPy-OH), which help in achieving nanocomposites containing well-distributed, exfoliated and undamaged MWCNTs. The thermal annealing at 100 °C of the pristine nanocomposite promotes the redistribution of the nanotubes in terms of a percolative network, thus converting the insulating material in a conducting soft matrix (60 μΩ m). This network remains unaltered after cooling to r.t. and successive heating cycles up to 100 °C thanks to the effective stabilization of MWCNTs provided by the functional polymer matrix. Notably, the resistivity-temperature profile is very reproducible and with a negative temperature coefficient of -0.002 K-1, which suggests the potential application of the composite as a temperature sensor. Overall, the industrial scale by which A-PPy-OH can be produced offers a straightforward alternative for the scale-up production of suitable polymers to generate multifunctional nanocomposites.