Cas no 1804986-61-5 (3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine)

3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine is a fluorinated pyridine derivative with a unique substitution pattern, offering versatile reactivity for pharmaceutical and agrochemical applications. The presence of both amino groups at the 3- and 4-positions enables selective functionalization, while the difluoromethyl and trifluoromethyl substituents enhance lipophilicity and metabolic stability. This compound serves as a valuable intermediate in the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and antimicrobial agents. Its electron-withdrawing trifluoromethyl group also facilitates nucleophilic aromatic substitution reactions, broadening its utility in heterocyclic chemistry. The structural features make it a promising candidate for further derivatization in drug discovery and material science research.
3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine structure
1804986-61-5 structure
Product Name:3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine
CAS No:1804986-61-5
MF:C7H6F5N3
MW:227.134658336639
CID:4850481
Update Time:2025-05-26

3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine Chemical and Physical Properties

Names and Identifiers

    • 3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine
    • Inchi: 1S/C7H6F5N3/c8-6(9)2-1-15-5(7(10,11)12)4(14)3(2)13/h1,6H,14H2,(H2,13,15)
    • InChI Key: SUQIJQDGRLEMAW-UHFFFAOYSA-N
    • SMILES: FC(C1=CN=C(C(F)(F)F)C(=C1N)N)F

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 1
  • Complexity: 219
  • XLogP3: 1
  • Topological Polar Surface Area: 64.9

3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A029073205-250mg
3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine
1804986-61-5 97%
250mg
$480.00 2022-04-01
Alichem
A029073205-500mg
3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine
1804986-61-5 97%
500mg
$815.00 2022-04-01
Alichem
A029073205-1g
3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine
1804986-61-5 97%
1g
$1,475.10 2022-04-01

Additional information on 3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine

3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine: A Comprehensive Overview

The compound 3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine (CAS No. 1804986-61-5) is a highly specialized organic molecule with significant potential in various chemical and pharmaceutical applications. This pyridine derivative features a unique combination of functional groups, including two amino groups at positions 3 and 4, a difluoromethyl group at position 5, and a trifluoromethyl group at position 2. These substituents contribute to its distinctive chemical properties and reactivity.

Recent studies have highlighted the importance of difluoromethyl and trifluoromethyl groups in modulating the electronic properties of aromatic compounds. The presence of these groups in 3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine enhances its stability and reactivity, making it a valuable precursor in the synthesis of advanced materials. For instance, researchers have explored its role in the development of novel polymers with improved thermal and mechanical properties.

The synthesis of 3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine involves a multi-step process that combines traditional organic synthesis techniques with modern catalytic methods. A key challenge in its production is the controlled introduction of the fluorinated substituents without compromising the integrity of the pyridine ring. Recent advancements in fluorination chemistry have provided more efficient pathways for this process, ensuring higher yields and better purity.

In terms of applications, this compound has shown promise in the field of medicinal chemistry. Its amino groups can act as nucleophilic sites for further functionalization, enabling the creation of bioactive molecules with tailored pharmacological properties. For example, studies have demonstrated its potential as a scaffold for developing inhibitors of key enzymes involved in neurodegenerative diseases.

The structural uniqueness of 3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine also makes it an attractive candidate for use in electronic materials. Its ability to undergo metal coordination has been leveraged in the design of metal-organic frameworks (MOFs) with enhanced conductivity and catalytic activity. These materials hold potential applications in energy storage and conversion technologies.

From an environmental perspective, understanding the degradation pathways of 3,4-Diamino-5-(difluoromethyl)-2-(trifluoromethyl)pyridine is crucial for assessing its ecological impact. Recent research has focused on its biodegradation under various environmental conditions, revealing that its fluorinated substituents influence both its persistence and toxicity.

In conclusion, 3,4-Diamino-5-(diffluromethy)-2-(trifluramethy)pyridine (CAS No. 1804986-61-5) is a versatile compound with a wide range of applications across multiple disciplines. Its unique structure and functional groups make it a valuable tool for advancing both fundamental research and industrial innovations. As ongoing studies continue to uncover new insights into its properties and potential uses, this compound is poised to play an increasingly important role in the development of next-generation materials and therapies.

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