Cas no 2672-57-3 (1,2,3-Benzenetricarboxylicacid, 1,2,3-trimethyl ester)
1,2,3-Benzenetricarboxylicacid, 1,2,3-trimethyl ester Chemical and Physical Properties
Names and Identifiers
-
- 1,2,3-Benzenetricarboxylicacid, 1,2,3-trimethyl ester
- Trimethyl 1,2,3-Benzenetricarboxylate
- 1,2,3-Benzenetricarboxylic acid trimethyl
- 1,2,3-benzenetricarboxylicacid,trimethylester
- 1.2.3-Benzoltricarboxylsaeuretrimethylester
- Benzene-1,2,3-tricarboxylic acid,trimethyl ester
- Benzol-1,2,3-tricarbonsaeure-trimethylester
- hemimelliticacid,trimethylester
- Hemimellitsaeure-trimethylester
- trimethyl benzene-1,2,3-tricarboxylate
- trimethyl hemimellitate
- DTXSID901334413
- SCHEMBL1666445
- SBOCVSUCRFVXFE-UHFFFAOYSA-N
- FT-0729136
- 1,2,3-trimethyl benzene-1,2,3-tricarboxylate
- 1,2,3-benzene-tricarboxylic acid trimethyl ester
- 1,2,3-benzenetricarboxylic acid, trimethyl ester
- AKOS016347550
- 2672-57-3
- Benzene-1,2,3-tricarboxylic acid, trimethyl ester
- benzene-1,2,3-tricarboxylic acid trimethyl ester
- TRIMETHYL1,2,3-BENZENETRICARBOXYLATE
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- Inchi: 1S/C12H12O6/c1-16-10(13)7-5-4-6-8(11(14)17-2)9(7)12(15)18-3/h4-6H,1-3H3
- InChI Key: SBOCVSUCRFVXFE-UHFFFAOYSA-N
- SMILES: O(C)C(C1C(C(=O)OC)=CC=CC=1C(=O)OC)=O
Computed Properties
- Exact Mass: 252.06300
- Monoisotopic Mass: 252.06338810g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 18
- Rotatable Bond Count: 6
- Complexity: 314
- 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
- Topological Polar Surface Area: 78.9?2
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
Experimental Properties
- Color/Form: Not available
- Density: 1.241
- Boiling Point: 291.2°C at 760 mmHg
- Flash Point: 123.2°C
- Refractive Index: 1.518
- PSA: 78.90000
- LogP: 1.04640
- Solubility: Not available
1,2,3-Benzenetricarboxylicacid, 1,2,3-trimethyl ester Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| City Chemical | 2317CC-1GM |
Trimethyl 1,2,3-Benzenetricarboxylate |
2672-57-3 | 97.0%(HPLC) | 1gm |
$309.54 | 2023-09-19 |
1,2,3-Benzenetricarboxylicacid, 1,2,3-trimethyl ester Related Literature
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H. V. Jain,D. Verthelyi,S. L. Beaucage RSC Adv., 2017,7, 42519-42528
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Andre Prates Pereira,Tao Dong,Eric P. Knoshaug,Nick Nagle,Ryan Spiller,Bonnie Panczak,Christopher J. Chuck,Philip T. Pienkos Sustainable Energy Fuels, 2020,4, 3400-3408
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Lei Yang,Yuan Zeng,Haibo Wu,Chunwu Zhou,Lei Tao J. Mater. Chem. B, 2020,8, 1383-1388
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Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580
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Kathrin Kutlescha,Rhett Kempe New J. Chem., 2010,34, 1954-1960
Additional information on 1,2,3-Benzenetricarboxylicacid, 1,2,3-trimethyl ester
1,2,3-Benzenetricarboxylic Acid, 1,2,3-Trimethyl Ester (CAS No: 2672-57-3)
The compound 1,2,3-benzenetricarboxylic acid, specifically its 1,2,3-trimethyl ester derivative (CAS No: 2672-57-3), is a highly versatile and intriguing molecule with applications spanning multiple disciplines. This compound is a derivative of benzenetricarboxylic acid, which serves as a foundational structure for various functional materials due to its unique chemical properties and structural features.
Recent advancements in materials science have highlighted the potential of benzenetricarboxylic acid derivatives in the development of advanced polymers and composites. The introduction of the trimethyl ester groups in this compound enhances its solubility in organic solvents, making it an ideal candidate for applications in polymer synthesis and high-performance materials. Researchers have demonstrated that this compound can be used as a building block for synthesizing high-strength polymers with exceptional thermal stability.
In the field of nanotechnology, the 1,2,3-trimethyl ester derivative has shown promise as a precursor for the synthesis of metal-organic frameworks (MOFs). These frameworks are widely used in gas storage, catalysis, and sensing applications due to their high surface area and tunable pore structures. The ability of this compound to coordinate with metal ions has been extensively studied in recent publications, underscoring its potential in creating novel MOF-based materials.
The synthesis of this compound involves a multi-step process that typically begins with the oxidation of suitable aromatic precursors followed by esterification reactions to introduce the methyl groups. Recent studies have optimized these reaction conditions to improve yield and purity, leveraging green chemistry principles to minimize environmental impact.
Beyond its material science applications, this compound has also garnered attention in pharmaceutical research. Its carboxylic acid groups can be modified to create bioactive molecules with potential therapeutic applications. For instance, derivatives of this compound have been explored as candidates for anti-inflammatory agents and antioxidants.
The structural integrity and reactivity of CAS No: 2672-57-3 make it a valuable tool in organic synthesis. Its ability to undergo various functional group transformations allows chemists to design molecules with tailored properties for specific applications. Recent research has focused on using this compound as a platform for synthesizing fluorescent probes and sensors for detecting environmental pollutants.
In summary, the compound 1,2,3-benzenetricarboxylic acid, particularly its 1,2,3-trimethyl ester, stands out as a multifaceted molecule with significant potential across diverse fields. Its unique chemical properties and versatility continue to drive innovative research directions in materials science and beyond.
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