Production Method 1

56-81-5

17171-71-0

141-93-5

629-50-5

99-62-7

496-11-7

1074-92-6

43133-95-5

590-18-1

527-84-4

1074-17-5

1595-11-5

700-12-9

1077-16-3

544-76-3

1595-09-1

2870-04-4

933-98-2

Reaction Conditions

1.1 Catalysts: Zinc ;  6 h, 1 bar, 420 °C

Reference

Renewable p-Xylene Production by Catalytic Conversion of Crude Bioglycerol (GTA-pX Process)

Singh, Vijendra ; Arumugam, Selvamani ; Kumar, Mahesh; Tathod, Anup Prakash; Viswanadham, Nagabhatla, Industrial & Engineering Chemistry Research, 2023, 62(4), 1788-1796

Benzene, 1,2-dipropyl- Raw materials

• Glycerol

Benzene, 1,2-dipropyl- Preparation Products

• 1,3-DIETHYLBENZENE (141-93-5)
• Tridecane (629-50-5)
• 1,3-Diisopropylbenzene (99-62-7)
• Benzene, 1,2-dipropyl- (17171-71-0)
• Indane (496-11-7)
• 1-tert-Butyl-2-methylbenzene (1074-92-6)
• Pentane, methyl- (43133-95-5)
• cis-2-Butene (590-18-1)
• o-Cymene (527-84-4)
• 1-Methyl-2-propylbenzene (1074-17-5)
• 2-Butyltoluene (1595-11-5)
• 1,2,3,4,5-pentamethylbenzene (700-12-9)
• Hexylbenzene (1077-16-3)
• Hexadecane (544-76-3)
• 1-methyl-4-pentylbenzene (1595-09-1)
• 2-Ethyl-m-xylene (2870-04-4)
• 1-Ethyl-2,3-dimethylbenzene (933-98-2)

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Benzene, 1,2-dipropyl- (CAS No. 17171-71-0): A Comprehensive Overview in Modern Chemical Research

Benzene, 1,2-dipropyl-, identified by its Chemical Abstracts Service (CAS) number 17171-71-0, is a significant compound in the realm of organic chemistry and pharmaceutical research. This substituted benzene derivative has garnered attention due to its unique structural properties and potential applications in various scientific domains. The presence of two propyl groups at the 1 and 2 positions introduces distinct electronic and steric effects, making it a valuable candidate for further investigation.

The molecular structure of Benzene, 1,2-dipropyl- consists of a benzene ring substituted with two propyl groups. This configuration imparts a certain degree of rigidity to the molecule while also influencing its reactivity and solubility characteristics. The propyl groups are alkyl substituents that can engage in various interactions with other molecules, including hydrogen bonding and hydrophobic effects. These interactions are crucial in determining the compound's behavior in different chemical environments.

In recent years, Benzene, 1,2-dipropyl- has been explored for its potential applications in pharmaceuticals. The benzene ring is a common motif in many bioactive molecules, and substituents like propyl groups can modulate the pharmacokinetic properties of these compounds. Researchers have been particularly interested in its role as a precursor or intermediate in the synthesis of more complex molecules. The ability to functionalize the benzene ring at specific positions allows for the creation of diverse chemical entities with tailored properties.

One of the most intriguing aspects of Benzene, 1,2-dipropyl- is its potential as a ligand in coordination chemistry. The benzene ring can act as a π-acceptor site, facilitating interactions with transition metals. Such metal complexes have been studied for their catalytic properties and their role in various industrial processes. The propyl groups can also influence the steric environment around the metal center, affecting the overall catalytic activity and selectivity.

The synthesis of Benzene, 1,2-dipropyl- typically involves Friedel-Crafts alkylation reactions on benzene using propyl halides or other suitable alkylating agents. Catalysts such as aluminum chloride or iron(III) chloride are often employed to facilitate these reactions. The choice of catalyst and reaction conditions can significantly impact the yield and purity of the final product. Recent advancements in green chemistry have also led to the exploration of more environmentally friendly synthetic routes, including catalytic systems that minimize waste and energy consumption.

From a biological perspective, Benzene, 1,2-dipropyl- has been investigated for its potential role as an intermediate in drug discovery. While not typically used as an active pharmaceutical ingredient itself, its structural framework provides insights into how substituents can influence biological activity. Computational modeling techniques have been employed to predict how this compound might interact with biological targets such as enzymes or receptors. These studies help guide the design of more potent and selective drugs based on similar molecular scaffolds.

The spectroscopic properties of Benzene, 1,2-dipropyl- make it an interesting subject for analytical chemistry research. Techniques such as nuclear magnetic resonance (NMR) spectroscopy and infrared (IR) spectroscopy provide detailed information about the molecular structure and dynamics. Mass spectrometry (MS) is also used to confirm the identity and purity of samples containing this compound. These analytical methods are essential for characterizing Benzene, 1,2-dipropyl- and understanding its behavior in different chemical systems.

In conclusion, Benzene, 1,2-dipropyl- (CAS No. 17171-71-0) is a versatile compound with significant implications in both synthetic chemistry and pharmaceutical research. Its unique structural features make it a valuable tool for studying molecular interactions and developing new chemical entities. As research continues to evolve, the applications of this compound are likely to expand further, contributing to advancements in various scientific fields.

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