Cas no 7210-27-7 (2-(Cyanomethyl)indole)

2-(Cyanomethyl)indole is a versatile indole derivative characterized by the presence of a cyanomethyl substituent at the 2-position of the indole scaffold. This compound serves as a valuable intermediate in organic synthesis, particularly in the construction of heterocyclic frameworks and pharmaceutical precursors. The reactive cyano group enhances its utility in nucleophilic addition and cyclization reactions, enabling the synthesis of complex indole-based structures. Its stability under standard conditions and compatibility with a range of reagents make it a practical choice for research and industrial applications. The compound is commonly employed in medicinal chemistry and materials science due to its modular reactivity and functional group tolerance.
2-(Cyanomethyl)indole structure
2-(Cyanomethyl)indole structure
Product Name:2-(Cyanomethyl)indole
CAS No:7210-27-7
MF:C10H8N2
MW:156.183921813965
CID:1017451
PubChem ID:169731
Update Time:2025-05-22

2-(Cyanomethyl)indole Chemical and Physical Properties

Names and Identifiers

    • 1H-Indole-2-acetonitrile
    • 2-(Cyanomethyl)indole
    • 1H-Indole-2-acetonitrile(9CI)
    • (2-Indolyl)acetonitril
    • 1H-indole-2ylacetonitrile
    • 2-(3-METHOXYPHENOXY)-5-(TRIFLUOROMETHYL)ANILINE
    • 2-Indoleacetonitrile
    • indol-2-yl acetonitrile
    • indole-2-acetonitrile
    • DTXSID80189483
    • 1H-indol-2-ylacetonitrile
    • FT-0665299
    • Indole-2-acetonitrile-13C2,15N
    • 35913-20-3
    • indol-2-yl-acetonitrile
    • SCHEMBL396373
    • 2-(1H-indol-2-yl)-acetonitrile
    • 2-(1H-indol-2-yl)acetonitrile
    • SCHEMBL2792039
    • RORMSTAFXZRNGK-UHFFFAOYSA-N
    • 1H-Indoleacetonitrile
    • AB45738
    • 7210-27-7
    • DB-260139
    • Inchi: 1S/C10H8N2/c11-6-5-9-7-8-3-1-2-4-10(8)12-9/h1-4,7,12H,5H2
    • InChI Key: RORMSTAFXZRNGK-UHFFFAOYSA-N
    • SMILES: N1C(CC#N)=CC2C=CC=CC1=2

Computed Properties

  • Exact Mass: 156.06900
  • Monoisotopic Mass: 156.068748264g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 203
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.8
  • Topological Polar Surface Area: 39.6?2

Experimental Properties

  • PSA: 39.58000
  • LogP: 2.23398

2-(Cyanomethyl)indole Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
C981920-25mg
2-(Cyanomethyl)indole
7210-27-7
25mg
$ 173.00 2023-09-08
TRC
C981920-250mg
2-(Cyanomethyl)indole
7210-27-7
250mg
$ 1357.00 2023-09-08
A2B Chem LLC
AH16901-25mg
2-(1H-Indol-2-yl)acetonitrile
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$289.00 2024-04-19
A2B Chem LLC
AH16901-250mg
2-(1H-Indol-2-yl)acetonitrile
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250mg
$1439.00 2024-04-19
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1629178-1g
2-(1H-indol-2-yl)acetonitrile
7210-27-7 98%
1g
¥6594.00 2024-05-02

Additional information on 2-(Cyanomethyl)indole

Comprehensive Overview of 2-(Cyanomethyl)indole (CAS No. 7210-27-7): Properties, Applications, and Industry Insights

2-(Cyanomethyl)indole (CAS No. 7210-27-7) is a versatile organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This heterocyclic molecule, characterized by its indole scaffold and cyanomethyl functional group, serves as a critical intermediate in the synthesis of bioactive compounds. Its unique structural features make it valuable for designing drug candidates, fluorescent probes, and specialty chemicals. Researchers frequently explore its reactivity in palladium-catalyzed cross-coupling reactions and multicomponent syntheses, aligning with the growing demand for efficient synthetic methodologies.

In recent years, the compound’s role in medicinal chemistry has been highlighted by its incorporation into kinase inhibitors and neuroprotective agents. The cyanomethyl moiety offers a strategic handle for further derivatization, enabling the development of compounds targeting cancer pathways and neurodegenerative diseases—topics trending in scientific literature and AI-driven drug discovery platforms. Additionally, its potential in material science, particularly for organic electronics, aligns with the surge in searches for sustainable materials and green chemistry alternatives.

The synthesis of 2-(Cyanomethyl)indole typically involves Knoevenagel condensation or nucleophilic substitution reactions, with optimization studies focusing on atom economy and catalyst recycling. These aspects resonate with industry priorities, as evidenced by frequent queries about cost-effective synthesis and waste reduction in organic production. Analytical characterization via NMR spectroscopy, HPLC purity testing, and mass spectrometry ensures compliance with stringent quality control standards, a recurring concern among manufacturers and regulatory bodies.

From a commercial perspective, 7210-27-7 is supplied by specialty chemical vendors under stringent Good Manufacturing Practices (GMP). Its pricing and availability are influenced by demand from contract research organizations (CROs) and academic laboratories, with supply chain discussions often centering on bulk customization and just-in-time delivery. The compound’s stability under ambient conditions and compatibility with common solvents like DMF and THF further enhance its utility in diverse applications.

Emerging trends also link 2-(Cyanomethyl)indole to machine learning-assisted molecular design, where its structural fingerprints are used to train algorithms for de novo drug discovery. This intersection of computational chemistry and experimental validation addresses frequent search queries about AI in chemical innovation. Furthermore, its ecological profile is under scrutiny, with studies evaluating biodegradation pathways to meet REACH compliance—a hotspot for ESG-focused enterprises.

In conclusion, 2-(Cyanomethyl)indole (CAS No. 7210-27-7) exemplifies the convergence of synthetic utility, therapeutic potential, and industrial relevance. Its adaptability to cutting-edge research domains ensures sustained interest, while its compliance with safety protocols and regulatory frameworks positions it as a reliable choice for modern chemical enterprises. As the scientific community prioritizes precision synthesis and multifunctional intermediates, this compound is poised to remain a cornerstone in advanced organic chemistry.

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