Cas no 32136-60-0 (Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate)

Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate is a versatile aromatic ester compound characterized by its three carboxylate groups and methoxy substituent. Its well-defined structure makes it valuable as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty polymers. The methoxy group enhances solubility in organic solvents, facilitating reactions under mild conditions. The ester functionalities provide reactive sites for further derivatization, enabling selective modifications. This compound exhibits stability under standard storage conditions, ensuring consistent performance in synthetic applications. Its high purity and predictable reactivity make it a preferred choice for researchers developing complex molecular architectures.
Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate structure
32136-60-0 structure
Product Name:Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate
CAS No:32136-60-0
MF:C13H14O7
MW:282.246064662933
CID:1092394
PubChem ID:72942156
Update Time:2025-10-05

Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate Chemical and Physical Properties

Names and Identifiers

    • Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate
    • Benzene-1,2,4-tricarboxylic acid, 5-methoxy, trimethyl ester
    • DTXSID301334384
    • Trimethyl5-methoxybenzene-1,2,4-tricarboxylate
    • 32136-60-0
    • AAUNKVZRYQTUNI-UHFFFAOYSA-N
    • Trimethyl 5-methoxy-1,2,4-benzenetricarboxylate
    • Inchi: 1S/C13H14O7/c1-17-10-6-8(12(15)19-3)7(11(14)18-2)5-9(10)13(16)20-4/h5-6H,1-4H3
    • InChI Key: AAUNKVZRYQTUNI-UHFFFAOYSA-N
    • SMILES: O(C)C1=CC(C(=O)OC)=C(C(=O)OC)C=C1C(=O)OC

Computed Properties

  • Exact Mass: 282.07392
  • Monoisotopic Mass: 282.07395278g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 7
  • Complexity: 379
  • 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: 1.5
  • Topological Polar Surface Area: 88.1?2

Experimental Properties

  • PSA: 88.13

Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A019086580-1g
Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate
32136-60-0 95%
1g
$321.44 2023-09-02
Crysdot LLC
CD12083995-1g
Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate
32136-60-0 95+%
1g
$402 2024-07-24

Additional information on Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate

Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate (CAS No. 32136-60-0): A Comprehensive Overview

Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate (CAS No. 32136-60-0) is a multifunctional organic compound that has garnered significant attention in the fields of organic synthesis, materials science, and pharmaceutical research. This compound is characterized by its unique molecular structure, which includes a benzene ring substituted with a methoxy group and three carboxylate groups esterified with methyl groups. The combination of these functional groups imparts a range of interesting chemical properties and potential applications.

The molecular formula of Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate is C15H16O7, and its molecular weight is approximately 308.30 g/mol. The compound is typically synthesized through a series of well-defined chemical reactions, including esterification and substitution reactions. The synthesis process can be optimized to achieve high yields and purity, making it suitable for various industrial and research applications.

In terms of physical properties, Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate is a white to off-white crystalline solid at room temperature. It is soluble in common organic solvents such as ethanol, methanol, and dichloromethane but has limited solubility in water. These solubility characteristics make it versatile for use in different solvent systems and reaction conditions.

The chemical stability of Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate is an important consideration for its practical applications. The compound is generally stable under normal storage conditions but can undergo hydrolysis in the presence of strong acids or bases. Therefore, it is recommended to store the compound in a dry and cool environment to maintain its integrity.

One of the key areas where Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate has shown significant potential is in the field of organic synthesis. The presence of multiple reactive functional groups makes it an excellent starting material for the synthesis of more complex molecules. For instance, recent studies have demonstrated the use of this compound as a building block for the synthesis of novel polymers and supramolecular assemblies. These materials exhibit unique properties such as high thermal stability and tunable optical properties, making them suitable for applications in electronics and photonics.

In the realm of materials science, Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate has been explored for its potential as a precursor for the preparation of metal-organic frameworks (MOFs). MOFs are highly porous materials with large surface areas that have found applications in gas storage, catalysis, and drug delivery. The ability to fine-tune the structure and properties of MOFs by using different organic linkers like Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate opens up new possibilities for their design and functionality.

In the pharmaceutical industry, Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate has been investigated as a potential lead compound for drug development. The methoxy group on the benzene ring can influence the compound's biological activity by modulating its lipophilicity and receptor binding affinity. Recent studies have shown that derivatives of this compound exhibit promising antitumor activity against various cancer cell lines. Additionally, the carboxylate groups can be modified to enhance the compound's solubility and bioavailability, making it more suitable for therapeutic applications.

The environmental impact of Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate is another important aspect to consider. While the compound itself is not classified as hazardous or toxic under current regulations, its production and use should be conducted with appropriate safety measures to minimize any potential environmental risks. Research into more sustainable synthesis methods and biodegradable derivatives is ongoing to address these concerns.

In conclusion, Trimethyl 5-methoxybenzene-1,2,4-tricarboxylate (CAS No. 32136-60-0) is a versatile organic compound with a wide range of applications in organic synthesis, materials science, and pharmaceutical research. Its unique molecular structure and chemical properties make it an attractive candidate for further exploration and development in these fields. As research continues to advance our understanding of this compound's potential uses and benefits, it is likely to play an increasingly important role in various scientific and industrial endeavors.

Recommended suppliers
Beyond Pharmaceutical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Changzhou Guanjia Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Changzhou Guanjia Chemical Co., Ltd
Shanghai Bent Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
鉅瀾化工科技(青島)有限公司
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
鉅瀾化工科技(青島)有限公司
Shenzhen Yaoyuan R&D Center Co.,Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shenzhen Yaoyuan R&D Center Co.,Ltd