Cas no 7313-22-6 (N,N,N',N'-Tetramethylmalonamide)
N,N,N',N'-Tetramethylmalonamide Chemical and Physical Properties
Names and Identifiers
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- n,n,n',n'-tetramethylmalonamide
- N,N,N',N'-tetramethylpropanediamide
- N,N,N',N'-Tetramethylmalonamid
- N,N,N',N'-tetramethyl-malonamide
- N,N,N',N'-Tetramethylmalonsaeurediamid
- N,N,N',N'-tetrametilmalonammide
- T1891
- N1,N1,N3,N3-Tetramethylmalonamide
- tetramethylmalonamide
- N,N,N,N-Tetramethylmalonamide
- AOXCXILUIVQCHH-UHFFFAOYSA-N
- N(1),N(1),N(3),N(3)-tetramethylmalonamide
- MFCD03093641
- 7313-22-6
- AS-62246
- CS-0455357
- DTXSID20450366
- AKOS027253011
- SCHEMBL283475
- H12001
- N,N,N'',N''-Tetramethylmalonamide
- N,N,N',N'-Tetramethylmalonamide
-
- MDL: MFCD03093641
- Inchi: 1S/C7H14N2O2/c1-8(2)6(10)5-7(11)9(3)4/h5H2,1-4H3
- InChI Key: AOXCXILUIVQCHH-UHFFFAOYSA-N
- SMILES: O=C(CC(N(C)C)=O)N(C)C
Computed Properties
- Exact Mass: 158.10600
- Monoisotopic Mass: 158.105527694g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 146
- 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
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: -0.6
- Topological Polar Surface Area: 40.6
Experimental Properties
- Color/Form: Not available
- Density: 1,1 g/cm3
- Boiling Point: 160°C/10mmHg(lit.)
- Flash Point: 113.4±15.0 °C
- Refractive Index: 1.4910-1.4940
- PSA: 40.62000
- LogP: -0.44710
- Solubility: Not available
- Vapor Pressure: 0.0±0.6 mmHg at 25°C
N,N,N',N'-Tetramethylmalonamide Security Information
-
Symbol:
- Prompt:warning
- Signal Word:warning
- Hazard Statement: H315-H319
- Warning Statement: P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
- Hazard Category Code: 36/37/38
- Safety Instruction: S26; S36/37/39
- Risk Phrases:R36/37/38
- Storage Condition:4° CStore…,-4℃Store…Better
N,N,N',N'-Tetramethylmalonamide Customs Data
- HS CODE:2924199090
- Customs Data:
China Customs Code:
2924199090Overview:
2924199090. Other acyclic amides(Including acyclic carbamates)(Including its derivatives and 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:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
N,N,N',N'-Tetramethylmalonamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | N159447-1g |
N,N,N',N'-Tetramethylmalonamide |
7313-22-6 | 97% | 1g |
¥92.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | N159447-25G |
N,N,N',N'-Tetramethylmalonamide |
7313-22-6 | 97% | 25g |
¥1567.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | N159447-5g |
N,N,N',N'-Tetramethylmalonamide |
7313-22-6 | 97% | 5g |
¥442.90 | 2023-09-01 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X72085-1g |
N1,N1,N3,N3-Tetramethylmalonamide |
7313-22-6 | ≥97% | 1g |
¥158.0 | 2023-09-05 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X72085-5g |
N1,N1,N3,N3-Tetramethylmalonamide |
7313-22-6 | ≥97% | 5g |
¥428.0 | 2023-09-05 | |
| abcr | AB144513-25 g |
N,N,N',N'-Tetramethylmalonamide, 97%; . |
7313-22-6 | 97% | 25g |
€233.30 | 2022-09-01 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | T1891-25G |
N,N,N',N'-Tetramethylmalonamide |
7313-22-6 | >97.0%(GC) | 25g |
¥1150.00 | 2024-04-16 | |
| Chemenu | CM313366-5g |
N1,N1,N3,N3-Tetramethylmalonamide |
7313-22-6 | 95% | 5g |
$*** | 2023-05-29 | |
| Chemenu | CM313366-25g |
N1,N1,N3,N3-Tetramethylmalonamide |
7313-22-6 | 95% | 25g |
$*** | 2023-05-29 | |
| Chemenu | CM313366-100g |
N1,N1,N3,N3-Tetramethylmalonamide |
7313-22-6 | 95% | 100g |
$*** | 2023-05-29 |
N,N,N',N'-Tetramethylmalonamide Suppliers
N,N,N',N'-Tetramethylmalonamide 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
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Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
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Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa Caccamo Phys. Chem. Chem. Phys., 2019,21, 11983-11991
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Eunkyung Choi,Minjoo Ryu,Haeri Lee,Ok-Sang Jung Dalton Trans., 2017,46, 4595-4601
Additional information on N,N,N',N'-Tetramethylmalonamide
N,N,N',N'-Tetramethylmalonamide (CAS No. 7313-22-6): An Overview of Its Properties, Applications, and Recent Research
N,N,N',N'-Tetramethylmalonamide (CAS No. 7313-22-6) is a versatile organic compound that has gained significant attention in various fields of chemistry and biochemistry. This compound, also known as TMM, is a derivative of malonamide with four methyl groups attached to the nitrogen atoms. Its unique structure and properties make it an important molecule in both academic research and industrial applications.
The chemical formula of N,N,N',N'-Tetramethylmalonamide is C8H16N2O2. It is a white crystalline solid at room temperature with a melting point of approximately 95-97°C. The compound is soluble in common organic solvents such as ethanol, methanol, and dichloromethane, but it has limited solubility in water. These physical properties make it suitable for a wide range of chemical reactions and processes.
In terms of its chemical structure, N,N,N',N'-Tetramethylmalonamide features a central malonamide core with four methyl groups attached to the nitrogen atoms. This configuration imparts several unique characteristics to the molecule, including enhanced stability and reactivity. The presence of the methyl groups also influences the compound's solubility and interaction with other molecules, making it a valuable building block in synthetic chemistry.
N,N,N',N'-Tetramethylmalonamide has found applications in various areas of chemistry and biochemistry. One of its primary uses is as an intermediate in the synthesis of more complex organic molecules. Its reactivity and stability make it an excellent starting material for the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, the compound's ability to form stable complexes with metal ions has led to its use in coordination chemistry and catalysis.
Recent research has explored the potential of N,N,N',N'-Tetramethylmalonamide in the development of new materials and pharmaceuticals. For instance, a study published in the Journal of Organic Chemistry highlighted the use of TMM as a key intermediate in the synthesis of novel antiviral agents. The researchers demonstrated that TMM can be efficiently converted into compounds with potent antiviral activity against several RNA viruses, including influenza and coronaviruses.
In another study, published in the Journal of Medicinal Chemistry, scientists investigated the use of N,N,N',N'-Tetramethylmalonamide in the development of new anticancer drugs. The study showed that TMM can be used to synthesize derivatives with enhanced cytotoxic activity against various cancer cell lines. The researchers noted that these derivatives exhibit improved selectivity and reduced toxicity compared to existing anticancer agents.
The versatility of N,N,N',N'-Tetramethylmalonamide extends beyond pharmaceutical applications. In materials science, TMM has been used as a building block for the synthesis of functional polymers and supramolecular assemblies. A recent study published in Macromolecules demonstrated that TMM can be polymerized to form highly ordered supramolecular structures with tunable properties. These structures have potential applications in areas such as drug delivery, sensing, and catalysis.
In addition to its synthetic applications, N,N,N',N'-Tetramethylmalonamide has been studied for its biological activities. Research has shown that TMM can modulate various biological processes, including enzyme activity and cell signaling pathways. For example, a study published in Bioorganic & Medicinal Chemistry Letters reported that TMM derivatives can inhibit specific enzymes involved in inflammatory responses, making them potential candidates for anti-inflammatory drugs.
The environmental impact of N,N,N',N'-Tetramethylmalonamide is another area of interest for researchers. Studies have investigated the biodegradability and ecotoxicity of TMM to ensure its safe use in industrial processes. A recent publication in Environmental Science & Technology indicated that TMM is biodegradable under aerobic conditions and does not pose significant environmental risks when used responsibly.
In conclusion, N,N,N',N'-Tetramethylmalonamide (CAS No. 7313-22-6) is a multifaceted compound with a wide range of applications in chemistry and biochemistry. Its unique structure and properties make it an invaluable tool for synthetic chemists, materials scientists, and pharmaceutical researchers. Ongoing research continues to uncover new uses for TMM, further solidifying its importance in these fields.
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