Cas no 117194-00-0 (2-formyl-N-methylbenzamide)

2-Formyl-N-methylbenzamide is a versatile aromatic aldehyde derivative with applications in organic synthesis and pharmaceutical intermediates. Its structure combines a formyl group with an N-methylbenzamide moiety, offering reactivity for condensation, nucleophilic addition, and cyclization reactions. The compound is particularly valued for its role in constructing heterocyclic frameworks and as a precursor in medicinal chemistry. Its well-defined molecular architecture ensures consistent performance in multi-step syntheses. The product is typically supplied with high purity, ensuring reliability in research and industrial processes. Proper handling under standard laboratory conditions is recommended due to its sensitivity to moisture and light.
2-formyl-N-methylbenzamide structure
2-formyl-N-methylbenzamide structure
Product Name:2-formyl-N-methylbenzamide
CAS No:117194-00-0
MF:C9H9NO2
MW:163.173262357712
CID:131515
PubChem ID:10844741
Update Time:2025-10-30

2-formyl-N-methylbenzamide Chemical and Physical Properties

Names and Identifiers

    • Benzamide,2-formyl-N-methyl-
    • 2-formyl-N-methylbenzamide
    • Benzamide, 2-formyl-N-methyl- (9CI)
    • SCHEMBL728983
    • 117194-00-0
    • DTXSID70445626
    • Z1068186268
    • EN300-1167041
    • Benzamide, 2-formyl-N-methyl-
    • Inchi: 1S/C9H9NO2/c1-10-9(12)8-5-3-2-4-7(8)6-11/h2-6H,1H3,(H,10,12)
    • InChI Key: VWBDIKTZQBRUKW-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC=CC=1C=O)NC

Computed Properties

  • Exact Mass: 163.06337
  • Monoisotopic Mass: 163.063328530g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 179
  • 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: 0.7
  • Topological Polar Surface Area: 46.2?2

Experimental Properties

  • PSA: 46.17

2-formyl-N-methylbenzamide Pricemore >>

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Additional information on 2-formyl-N-methylbenzamide

Comprehensive Overview of 2-Formyl-N-methylbenzamide (CAS No. 117194-00-0): Properties, Applications, and Industry Insights

2-Formyl-N-methylbenzamide (CAS No. 117194-00-0) is a specialized organic compound widely recognized for its versatile applications in pharmaceutical intermediates, agrochemical synthesis, and material science. This aromatic aldehyde-amide hybrid features a formyl group (-CHO) and an N-methylbenzamide moiety, making it a valuable building block in modern synthetic chemistry. With the rising demand for high-purity intermediates in drug discovery, this compound has garnered significant attention from researchers and manufacturers alike.

In recent years, the compound’s role in green chemistry and sustainable synthesis has become a focal point. As industries shift toward eco-friendly processes, 2-formyl-N-methylbenzamide is increasingly studied for its potential in catalytic reactions and biodegradable material design. Searches for terms like "biodegradable amides" and "non-toxic aromatic aldehydes" have surged, reflecting growing environmental concerns among users. Its low toxicity profile and compatibility with microwave-assisted synthesis further enhance its appeal.

The structural uniqueness of CAS No. 117194-00-0 lies in its dual functional groups, enabling diverse reactivity. The formyl group participates in condensation reactions, while the N-methylamide segment offers hydrogen-bonding capabilities. This duality supports applications in heterocyclic compound synthesis, a trending topic in pharmaceutical forums. Queries such as "amide-based drug intermediates 2024" and "formyl derivatives in medicinal chemistry" highlight its relevance in cutting-edge research.

From a commercial perspective, 2-formyl-N-methylbenzamide is often sourced as a white to off-white crystalline powder with high purity (>98%). Analytical techniques like HPLC and NMR spectroscopy are critical for quality control, aligning with industry standards for GMP-compliant intermediates. Discussions around "HPLC methods for amide analysis" and "spectroscopic characterization of aldehydes" frequently appear in technical literature, underscoring the compound’s analytical importance.

Emerging trends also link 117194-00-0 to catalysis innovation. Researchers explore its use in palladium-catalyzed cross-coupling and photoredox reactions, addressing the demand for efficient synthetic routes. Notably, its stability under mild conditions makes it suitable for flow chemistry systems, a hot topic in process optimization circles. Searches for "continuous flow amide synthesis" or "scalable aldehyde reactions" reflect this industrial shift.

In conclusion, 2-formyl-N-methylbenzamide (CAS No. 117194-00-0) exemplifies the intersection of functionality and sustainability. Its adaptability across pharmaceuticals, agrochemicals, and advanced materials ensures enduring relevance. As the scientific community prioritizes atom-efficient synthesis and green solvents, this compound is poised to remain a key player in innovative chemistry solutions.

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