Cas no 117194-00-0 (2-formyl-N-methylbenzamide)
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 >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1167041-0.05g |
2-formyl-N-methylbenzamide |
117194-00-0 | 95% | 0.05g |
$118.0 | 2023-06-08 | |
| Enamine | EN300-1167041-0.1g |
2-formyl-N-methylbenzamide |
117194-00-0 | 95% | 0.1g |
$176.0 | 2023-06-08 | |
| Enamine | EN300-1167041-0.25g |
2-formyl-N-methylbenzamide |
117194-00-0 | 95% | 0.25g |
$252.0 | 2023-06-08 | |
| Enamine | EN300-1167041-0.5g |
2-formyl-N-methylbenzamide |
117194-00-0 | 95% | 0.5g |
$457.0 | 2023-06-08 | |
| Enamine | EN300-1167041-1.0g |
2-formyl-N-methylbenzamide |
117194-00-0 | 95% | 1g |
$584.0 | 2023-06-08 | |
| Enamine | EN300-1167041-2.5g |
2-formyl-N-methylbenzamide |
117194-00-0 | 95% | 2.5g |
$1147.0 | 2023-06-08 | |
| Enamine | EN300-1167041-5.0g |
2-formyl-N-methylbenzamide |
117194-00-0 | 95% | 5g |
$1695.0 | 2023-06-08 | |
| Enamine | EN300-1167041-10.0g |
2-formyl-N-methylbenzamide |
117194-00-0 | 95% | 10g |
$2516.0 | 2023-06-08 | |
| Enamine | EN300-1167041-50mg |
2-formyl-N-methylbenzamide |
117194-00-0 | 95.0% | 50mg |
$118.0 | 2023-10-03 | |
| Enamine | EN300-1167041-100mg |
2-formyl-N-methylbenzamide |
117194-00-0 | 95.0% | 100mg |
$176.0 | 2023-10-03 |
2-formyl-N-methylbenzamide Related Literature
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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4. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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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