Cas no 91896-86-5 (Benzenemethanamine, a-methyl-a-propyl-)

Benzenemethanamine, a-methyl-a-propyl- structure
91896-86-5 structure
Product Name:Benzenemethanamine, a-methyl-a-propyl-
CAS No:91896-86-5
MF:C11H17N
MW:163.259382963181
CID:4665033
Update Time:2025-07-01

Benzenemethanamine, a-methyl-a-propyl- Chemical and Physical Properties

Names and Identifiers

    • α-Methyl-α-propylbenzenemethanamine
    • 2-Phenylpentan-2-amine
    • Benzenemethanamine, a-methyl-a-propyl-
    • Inchi: 1S/C11H17N/c1-3-9-11(2,12)10-7-5-4-6-8-10/h4-8H,3,9,12H2,1-2H3
    • InChI Key: UYHZEICCELUQFG-UHFFFAOYSA-N
    • SMILES: C1(C(N)(C)CCC)=CC=CC=C1

Benzenemethanamine, a-methyl-a-propyl- Pricemore >>

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Additional information on Benzenemethanamine, a-methyl-a-propyl-

Benzenemethanamine, a-Methyl-a-Propyl

Benzenemethanamine, a-methyl-a-propyl (CAS No. 91896-86-5) is an organic compound with the molecular formula C10H17N. This compound belongs to the class of secondary amines and is derived from benzene with specific substituents. The structure of Benzenemethanamine, a-methyl-a-propyl consists of a benzene ring attached to a methanamine group, where the nitrogen atom is further substituted with both methyl and propyl groups. This unique structure gives the compound its distinct chemical properties and makes it an interesting subject for both academic and industrial research.

Recent studies have highlighted the potential applications of Benzenemethanamine, a-methyl-a-propyl in various fields, including pharmaceuticals, agrochemicals, and materials science. For instance, researchers have explored its role as an intermediate in the synthesis of bioactive compounds. The compound's ability to form stable bonds with other molecules has made it a valuable building block in drug discovery programs targeting specific therapeutic areas such as oncology and neurodegenerative diseases.

The synthesis of Benzenemethanamine, a-methyl-a-propyl involves multi-step reactions that require precise control over reaction conditions to achieve high yields and purity. One common approach involves the alkylation of aniline derivatives followed by reduction and subsequent substitution reactions. Advanced techniques such as microwave-assisted synthesis and catalytic hydrogenation have been employed to optimize the production process, ensuring scalability for industrial applications.

In terms of physical properties, Benzenemethanamine, a-methyl-a-propyl is typically a white crystalline solid with a melting point around 70°C. It is sparingly soluble in water but dissolves readily in organic solvents such as dichloromethane and ethanol. These solubility characteristics make it suitable for use in various organic reactions where phase separation or extraction techniques are employed.

From an environmental perspective, understanding the fate and behavior of Benzenemethanamine, a-methyl-a-propyl in natural systems is crucial for assessing its potential impact on ecosystems. Recent environmental studies have focused on its biodegradation pathways under aerobic and anaerobic conditions. Results indicate that the compound undergoes microbial degradation through enzymatic hydrolysis, leading to the formation of less complex organic molecules that are eventually mineralized into carbon dioxide and water.

Moreover, Benzenemethanamine, a-methyl-a-propyl has been investigated for its role in green chemistry initiatives. Its ability to participate in catalytic cycles without generating harmful byproducts aligns with the principles of sustainable chemical manufacturing. Researchers are exploring its potential as a catalyst in asymmetric synthesis reactions, which could significantly reduce waste generation and energy consumption in industrial processes.

In conclusion, Benzenemethanamine, a-methyl-a-propyl (CAS No. 91896-86-5) is a versatile compound with promising applications across multiple disciplines. Its unique chemical structure, combined with advancements in synthetic methodologies and environmental assessments, positions it as a key player in modern chemical research and development.

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