Cas no 13698-87-8 (NNN'N'-Tetraethylisophthalamide)
NNN'N'-Tetraethylisophthalamide Chemical and Physical Properties
Names and Identifiers
-
- 1,3-Benzenedicarboxamide,N1,N1,N3,N3-tetraethyl-
- 1-N,1-N,3-N,3-N-tetraethylbenzene-1,3-dicarboxamide
- N N N N-TETRAETHYLISOPHTHALAMIDE
- NNN'N'-TETRAETHYLISOPHTHALAMIDE
- [3-(N,N-diethylcarbamoyl)phenyl]-N,N-diethylcarboxamide
- isophthaloyl bis(diethylamide)
- Isophthalsaeure-bis-diaethylamid
- N,N,N',N'-tetraethyl-1,3-benzenedicarboxamide
- Tetra-N-aethyl-isophthalamid
- tetra-N-ethyl-isophthalamide
- TIMTEC-BB SBB007918
- 1,3-BenzenedicarboxaMide, N,N,N',N'-tetraethyl-
- SR-01000478048-1
- GZWCNZZTWDDVSL-UHFFFAOYSA-N
- N1,N1,N3,N3-tetraethylisophthalamide
- FT-0676073
- N1,N1,N3,N3-tetraethylbenzene-1,3-dicarboxamide
- DTXSID90333834
- TimTec1_003026
- SCHEMBL7406512
- Oprea1_104559
- EU-0009815
- NNN/'N/'-TETRAETHYLISOPHTHALAMIDE
- MFCD00043652
- 1,3-Benzenedicarboxamide, N1,N1,N3,N3-tetraethyl-
- SR-01000478048
- BRD-K51473477-001-01-4
- N,N,N',N'-Tetraethylisophthalamide
- CHEMBL4580981
- 13698-87-8
- HMS1542J12
- AKOS003265986
- NNN'N'-Tetraethylisophthalamide
-
- MDL: MFCD00043652
- Inchi: 1S/C16H24N2O2/c1-5-17(6-2)15(19)13-10-9-11-14(12-13)16(20)18(7-3)8-4/h9-12H,5-8H2,1-4H3
- InChI Key: GZWCNZZTWDDVSL-UHFFFAOYSA-N
- SMILES: O=C(C1C=CC=C(C=1)C(N(CC)CC)=O)N(CC)CC
Computed Properties
- Exact Mass: 276.18400
- Monoisotopic Mass: 276.183778013g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 20
- Rotatable Bond Count: 8
- Complexity: 292
- 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: 1.4
- Topological Polar Surface Area: 40.6?2
Experimental Properties
- Density: 1.0209 (rough estimate)
- Melting Point: 86°C
- Boiling Point: 419.28°C (rough estimate)
- Flash Point: 198.2±16.4 °C
- Refractive Index: 1.5800 (estimate)
- PSA: 40.62000
- LogP: 2.65060
- Vapor Pressure: 0.0±1.1 mmHg at 25°C
NNN'N'-Tetraethylisophthalamide Security Information
- Signal Word:warning
- Hazard Statement: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
NNN'N'-Tetraethylisophthalamide Customs Data
- HS CODE:2924299090
- Customs Data:
China Customs Code:
2924299090Overview:
2924299090. Other cyclic amides(Including cyclic carbamates)(Including their derivatives as well as their salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, packing
Summary:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
NNN'N'-Tetraethylisophthalamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB357634-5 g |
NNN'N'-Tetraethylisophthalamide |
13698-87-8 | 5g |
€129.70 | 2022-08-31 | ||
| abcr | AB357634-25 g |
NNN'N'-Tetraethylisophthalamide |
13698-87-8 | 25g |
€391.50 | 2022-08-31 | ||
| TRC | P271010-50mg |
NNN'N'-Tetraethylisophthalamide |
13698-87-8 | 50mg |
$ 50.00 | 2022-06-03 | ||
| TRC | P271010-100mg |
NNN'N'-Tetraethylisophthalamide |
13698-87-8 | 100mg |
$ 65.00 | 2022-06-03 | ||
| TRC | P271010-500mg |
NNN'N'-Tetraethylisophthalamide |
13698-87-8 | 500mg |
$ 80.00 | 2022-06-03 | ||
| abcr | AB357634-5g |
NNN'N'-Tetraethylisophthalamide; . |
13698-87-8 | 5g |
€141.50 | 2025-04-21 | ||
| abcr | AB357634-25g |
NNN'N'-Tetraethylisophthalamide; . |
13698-87-8 | 25g |
€422.00 | 2025-04-21 | ||
| 1PlusChem | 1P001342-5g |
1,3-Benzenedicarboxamide, N1,N1,N3,N3-tetraethyl- |
13698-87-8 | 5g |
$114.00 | 2023-12-22 | ||
| 1PlusChem | 1P001342-25g |
1,3-Benzenedicarboxamide, N1,N1,N3,N3-tetraethyl- |
13698-87-8 | 25g |
$327.00 | 2023-12-22 | ||
| A2B Chem LLC | AA49890-5g |
1,3-Benzenedicarboxamide, N1,N1,N3,N3-tetraethyl- |
13698-87-8 | 5g |
$107.00 | 2024-04-20 |
NNN'N'-Tetraethylisophthalamide Suppliers
NNN'N'-Tetraethylisophthalamide Related Literature
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
-
Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
-
Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
Additional information on NNN'N'-Tetraethylisophthalamide
Chemical Profile of NNN'N'-Tetraethylisophthalamide (CAS No. 13698-87-8)
NNN'N'-Tetraethylisophthalamide, identified by the chemical identifier CAS No. 13698-87-8, is a compound of significant interest in the field of organic chemistry and pharmaceutical research. This tetraethyl derivative of isophthalamic acid exhibits unique structural and functional properties that have positioned it as a subject of extensive investigation in both academic and industrial settings. The compound’s molecular framework, characterized by its four ethyl substituents, contributes to its distinct reactivity and potential applications in synthetic chemistry and material science.
The structural motif of NNN'N'-Tetraethylisophthalamide is derived from isophthalic acid, a dicarboxylic acid known for its role in the synthesis of various polymeric materials and pharmaceutical intermediates. The introduction of ethyl groups at the nitrogen positions enhances the compound’s solubility and stability, making it more amenable to further functionalization and derivatization. This adaptability has garnered attention from researchers exploring novel methodologies in drug development and polymer chemistry.
In recent years, advancements in computational chemistry have enabled more precise predictions of the behavior of such complex molecules. Studies utilizing molecular modeling techniques have revealed that NNN'N'-Tetraethylisophthalamide possesses a high degree of conformational flexibility, which could be exploited in the design of molecular recognition systems. This flexibility, combined with its ability to participate in hydrogen bonding interactions, makes it a promising candidate for applications in enzyme inhibition studies and as a ligand in coordination chemistry.
One of the most compelling areas of research involving NNN'N'-Tetraethylisophthalamide is its potential role as an intermediate in the synthesis of bioactive molecules. Researchers have demonstrated its utility in constructing heterocyclic scaffolds, which are prevalent in many pharmacologically active compounds. The tetraethyl group provides a reactive handle for further modifications, allowing chemists to tailor the molecule’s properties for specific biological targets. For instance, modifications at the ethyl positions can fine-tune electronic effects and steric hindrance, influencing binding affinity and metabolic stability.
The pharmaceutical industry has been particularly intrigued by the potential of NNN'N'-Tetraethylisophthalamide as a building block for novel therapeutic agents. Preliminary studies suggest that derivatives of this compound may exhibit inhibitory activity against certain enzymes implicated in metabolic disorders. By leveraging structure-activity relationship (SAR) studies, researchers aim to optimize the molecule’s pharmacokinetic profile, enhancing its suitability for clinical applications. The compound’s compatibility with green chemistry principles has also been noted, as its synthesis can be achieved under mild conditions with minimal waste generation.
Beyond pharmaceutical applications, NNN'N'-Tetraethylisophthalamide has shown promise in materials science. Its ability to form stable complexes with metal ions has been explored for the development of new catalysts and sensors. These complexes exhibit enhanced catalytic activity in various organic transformations, including cross-coupling reactions and oxidation processes. Additionally, the compound’s thermal stability makes it a candidate for high-performance polymers, where it can serve as a cross-linking agent or modifier to improve material properties such as tensile strength and heat resistance.
The synthesis of NNN'N'-Tetraethylisophthalamide typically involves multi-step reactions starting from commercially available precursors such as diethyl isophthalate or isophthalic acid derivatives. Advances in synthetic methodologies have refined these processes, reducing reaction times and improving yields. Catalytic techniques, including transition metal-catalyzed reactions, have been particularly effective in streamlining the synthesis while maintaining high purity standards. Such improvements are crucial for scaling up production and ensuring consistency for industrial applications.
Recent research has also highlighted the importance of understanding the environmental impact of chemical processes involving NNN'N'-Tetraethylisophthalamide. Efforts to develop sustainable synthetic routes have focused on reducing energy consumption and minimizing hazardous byproducts. Green solvent systems, such as supercritical fluids or ionic liquids, have been investigated as alternatives to traditional organic solvents, offering a more environmentally benign approach to production.
In conclusion,NNN'N'-Tetraethylisophthalamide (CAS No. 13698-87-8) represents a versatile compound with broad applications across multiple scientific disciplines. Its unique structural features make it an attractive candidate for drug discovery, polymer science, and catalysis. As research continues to uncover new methodologies for its synthesis and application,NNN'N'-Tetraethylisophthalamide is poised to play an increasingly significant role in advancing both fundamental science and industrial innovation.
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