Cas no 2270913-44-3 (Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester)

Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester structure
2270913-44-3 structure
Product Name:Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester
CAS No:2270913-44-3
MF:C12H10ClN3O2
MW:263.679701328278
MDL:MFCD31700286
CID:4783393
Update Time:2025-07-09

Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester Chemical and Physical Properties

Names and Identifiers

    • Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester
    • MDL： MFCD31700286
    • Inchi： 1S/C12H10ClN3O2/c1-18-12(17)8-4-2-7(3-5-8)9-6-10(13)15-16-11(9)14/h2-6H,1H3,(H2,14,16)
    • InChI Key： WOWAKOOPDKOHJU-UHFFFAOYSA-N
    • SMILES： C(OC)(=O)C1=CC=C(C2=CC(Cl)=NN=C2N)C=C1

Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Matrix Scientific
190728-2.500g
4-(3-Amino-6-chloropyridazin-4-yl)-benzoic acid methyl ester, 95%
 2270913-44-3 95%
2.500g
 $1650.00 2023-09-10

Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester Related Literature

Additional information on Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester

Benzoic Acid, 4-(3-Amino-6-Chloro-4-Pyridazinyl)-, Methyl Ester: A Comprehensive Overview

The compound Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester, with the CAS number 2270913-44-3, is a significant molecule in the field of organic chemistry and pharmacology. This compound has garnered attention due to its unique structural features and potential applications in drug development and material science. The molecule consists of a benzoic acid moiety substituted at the para position with a pyridazine ring that carries both amino and chloro substituents. The methyl ester group further enhances its chemical versatility.

The synthesis of this compound involves a series of carefully designed reactions, including nucleophilic aromatic substitution and coupling reactions. Recent studies have focused on optimizing the synthesis pathway to improve yield and purity, making it more accessible for large-scale production. The compound's structure is particularly interesting due to the presence of the pyridazine ring, which is known for its aromaticity and ability to participate in various chemical reactions.

One of the most promising applications of this compound lies in its potential as a building block for drug discovery. The amino group on the pyridazine ring can act as a site for further functionalization, enabling the creation of bioactive molecules with specific pharmacological properties. For instance, researchers have explored its use in designing inhibitors for certain enzymes involved in disease pathways.

In addition to its role in pharmaceuticals, this compound has also been investigated for its electronic properties. The conjugated system formed by the benzoic acid and pyridazine moieties contributes to its ability to absorb light in the visible spectrum, making it a candidate for applications in optoelectronics and photovoltaics.

Recent advancements in computational chemistry have allowed for detailed studies of this compound's electronic structure and reactivity. These studies have provided insights into its stability under various conditions and its potential interactions with biological systems.

In conclusion, Benzoic acid, 4-(3-amino-6-chloro-4-pyridazinyl)-, methyl ester is a versatile compound with a wide range of potential applications. Its unique structure and reactivity make it an invaluable tool in both academic research and industrial development.

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