Cas no 35042-26-3 (2,6-Pyrazinedicarboxylicacid, 2,6-dimethyl ester)

2,6-Pyrazinedicarboxylic acid, 2,6-dimethyl ester, is a pyrazine-based diester compound with applications in organic synthesis and pharmaceutical intermediates. Its key advantages include high purity and stability, making it suitable for use in controlled reactions. The dimethyl ester group enhances solubility in organic solvents, facilitating its incorporation into complex molecular frameworks. The compound’s rigid pyrazine core provides structural versatility for constructing heterocyclic systems. It is commonly employed in the synthesis of ligands, coordination complexes, and bioactive molecules due to its well-defined reactivity. Proper handling under standard laboratory conditions ensures consistent performance in synthetic workflows.
2,6-Pyrazinedicarboxylicacid, 2,6-dimethyl ester structure
35042-26-3 structure
Product Name:2,6-Pyrazinedicarboxylicacid, 2,6-dimethyl ester
CAS No:35042-26-3
MF:C8H8N2O4
MW:196.160121917725
CID:295292
PubChem ID:14715227
Update Time:2025-05-25

2,6-Pyrazinedicarboxylicacid, 2,6-dimethyl ester Chemical and Physical Properties

Names and Identifiers

    • 2,6-Pyrazinedicarboxylicacid, 2,6-dimethyl ester
    • DIMETHYL PYRAZINE-2,6-DICARBOXYLATE
    • 2,6-dimethoxycarbonylpyrazine
    • 2,6-Pyrazinedicarboxylic acid,dimethyl ester
    • 6-Acetoxy-pyrazin-2-carbonsaeure-methyl-ester
    • Dimethyl2,6-pyrazinedicarboxylate
    • Pyrazin-2,6-dicarbonsaeure-dimethylester
    • Pyrazin-2,6-dicarbonsaeure-methylester
    • pyrazine-2,6-dicarboxylic acid dimethyl ester
    • RSXGKDUYJPQZTL-UHFFFAOYSA-N
    • 2,6-DIMETHYL PYRAZINE-2,6-DICARBOXYLATE
    • AKOS006290535
    • E83618
    • EN300-8583720
    • 35042-26-3
    • SCHEMBL69342
    • DTXSID80563289
    • Inchi: 1S/C8H8N2O4/c1-13-7(11)5-3-9-4-6(10-5)8(12)14-2/h3-4H,1-2H3
    • InChI Key: RSXGKDUYJPQZTL-UHFFFAOYSA-N
    • SMILES: O(C)C(C1C=NC=C(C(=O)OC)N=1)=O

Computed Properties

  • Exact Mass: 196.04800
  • Monoisotopic Mass: 196.04840674g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 4
  • Complexity: 209
  • 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: -0.3
  • Topological Polar Surface Area: 78.4?2

Experimental Properties

  • PSA: 78.38000
  • LogP: 0.04980

2,6-Pyrazinedicarboxylicacid, 2,6-dimethyl ester Customs Data

  • HS CODE:2933990090
  • Customs Data:

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

2,6-Pyrazinedicarboxylicacid, 2,6-dimethyl ester Pricemore >>

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Additional information on 2,6-Pyrazinedicarboxylicacid, 2,6-dimethyl ester

2,6-Pyrazinedicarboxylic Acid, 2,6-Dimethyl Ester: A Comprehensive Overview

The compound with CAS No. 35042-26-3, commonly referred to as 2,6-pyrazinedicarboxylic acid, 2,6-dimethyl ester, is a significant molecule in the field of organic chemistry. This compound belongs to the class of pyrazine derivatives and has garnered attention due to its unique chemical properties and potential applications in various industries. The pyrazine ring serves as the core structure, with two carboxylic acid groups substituted at the 2 and 6 positions. These groups are further esterified with methyl groups, forming the dimethyl ester derivative.

Recent studies have highlighted the importance of pyrazine derivatives in material science and pharmacology. The pyrazine ring is known for its aromatic stability and ability to participate in various chemical reactions, making it a versatile building block for synthesizing complex molecules. The dimethyl ester groups in this compound contribute to its solubility and reactivity, which are crucial for its applications in organic synthesis and catalysis.

One of the most promising areas of research involving 2,6-pyrazinedicarboxylic acid, 2,6-dimethyl ester is its role in drug development. Scientists have explored its potential as a precursor for synthesizing bioactive compounds with anti-inflammatory and antioxidant properties. For instance, a study published in *Journal of Medicinal Chemistry* demonstrated that derivatives of this compound exhibit significant activity against certain enzymes involved in inflammatory pathways.

In addition to its pharmacological applications, this compound has also found utility in the field of materials science. Researchers have investigated its ability to form coordination polymers and metal-organic frameworks (MOFs). The carboxylate groups in the molecule can act as ligands, enabling the formation of stable structures with metal ions. This property makes it a valuable component in the development of advanced materials for gas storage and catalysis.

The synthesis of 2,6-pyrazinedicarboxylic acid, 2,6-dimethyl ester typically involves multi-step organic reactions. A common approach includes the oxidation of a suitable pyrazine derivative followed by esterification. Recent advancements in catalytic methods have improved the efficiency and selectivity of these reactions, leading to higher yields and purer products.

From an environmental perspective, this compound has been studied for its biodegradability and eco-friendly properties. Research indicates that under specific conditions, it can undergo microbial degradation without releasing harmful byproducts. This makes it a safer alternative for industrial applications compared to some traditional chemicals.

In conclusion, 2,6-pyrazinedicarboxylic acid, 2,6-dimethyl ester (CAS No. 35042-26-3) is a versatile compound with a wide range of applications across different scientific domains. Its unique chemical structure and functional groups make it an invaluable tool in organic synthesis, drug discovery, and materials science. As ongoing research continues to uncover new properties and uses for this compound, its significance in both academic and industrial settings is expected to grow further.

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