Cas no 64379-44-8 (1,5-naphthyridine-4-carbaldehyde)
1,5-naphthyridine-4-carbaldehyde Chemical and Physical Properties
Names and Identifiers
-
- 1,5-Naphthyridine-4-carboxaldehyde
- [1,5]Naphthyridine-4-carbaldehyde
- 1,5-NAPHTHYRIDINE-4-CARBALDEHYDE
- XROYXOXXNKCIDA-UHFFFAOYSA-N
- E78566
- EN300-2998366
- CS-0454526
- BS-49457
- DTXSID30696733
- Z1255468088
- 64379-44-8
- DB-345559
- SCHEMBL1717340
- 1,5-naphthyridine-4-carbaldehyde
-
- MDL: MFCD18073225
- Inchi: 1S/C9H6N2O/c12-6-7-3-5-10-8-2-1-4-11-9(7)8/h1-6H
- InChI Key: XROYXOXXNKCIDA-UHFFFAOYSA-N
- SMILES: O=CC1=CC=NC2=CC=CN=C21
Computed Properties
- Exact Mass: 158.04808
- Monoisotopic Mass: 158.048012819g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 12
- Rotatable Bond Count: 1
- Complexity: 172
- 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: 0.7
- Topological Polar Surface Area: 42.8?2
Experimental Properties
- PSA: 42.85
1,5-naphthyridine-4-carbaldehyde Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM123399-1g |
1,5-naphthyridine-4-carbaldehyde |
64379-44-8 | 95% | 1g |
$333 | 2021-08-05 | |
| Chemenu | CM123399-250mg |
1,5-naphthyridine-4-carbaldehyde |
64379-44-8 | 95% | 250mg |
$*** | 2023-05-30 | |
| Chemenu | CM123399-1g |
1,5-naphthyridine-4-carbaldehyde |
64379-44-8 | 95% | 1g |
$*** | 2023-05-30 | |
| Ambeed | A219307-50mg |
1,5-Naphthyridine-4-carbaldehyde |
64379-44-8 | 98% | 50mg |
$231.0 | 2025-04-18 | |
| Ambeed | A219307-100mg |
1,5-Naphthyridine-4-carbaldehyde |
64379-44-8 | 98% | 100mg |
$378.0 | 2025-04-18 | |
| Ambeed | A219307-250mg |
1,5-Naphthyridine-4-carbaldehyde |
64379-44-8 | 98% | 250mg |
$632.0 | 2025-04-18 | |
| Ambeed | A219307-1g |
1,5-Naphthyridine-4-carbaldehyde |
64379-44-8 | 98% | 1g |
$764.0 | 2025-04-18 | |
| eNovation Chemicals LLC | Y1216765-1g |
1,5-Naphthyridine-4-carbaldehyde |
64379-44-8 | 95% | 1g |
$1200 | 2024-06-03 | |
| Alichem | A219008025-1g |
1,5-Naphthyridine-4-carbaldehyde |
64379-44-8 | 95% | 1g |
$400.00 | 2023-09-01 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBTQ3748-1G |
1,5-naphthyridine-4-carbaldehyde |
64379-44-8 | 95% | 1g |
¥ 1,656.00 | 2023-04-03 |
1,5-naphthyridine-4-carbaldehyde Related Literature
-
Fuming Xiao,Mengzhu Wang,Yunxiang Lei,Wenbo Dai,Yunbing Zhou,Miaochang Liu,Wenxia Gao,Xiaobo Huang,Huayue Wu J. Mater. Chem. C, 2020,8, 17410-17416
-
Shivani Sharma,Chia-Ming Wu,Ranjit T. Koodali,N. Rajesh RSC Adv., 2016,6, 26668-26678
-
Chandran Rajendran,Govindaswamy Satishkumar,Charlotte Lang,Eric M. Gaigneaux Catal. Sci. Technol., 2020,10, 2583-2592
-
Yaqing Liu,Jiangtao Ren,Jing Li,Jiyang Liu,Erkang Wang Chem. Commun., 2012,48, 802-804
-
Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
Additional information on 1,5-naphthyridine-4-carbaldehyde
Introduction to 1,5-naphthyridine-4-carbaldehyde (CAS No. 64379-44-8)
1,5-naphthyridine-4-carbaldehyde, identified by the Chemical Abstracts Service Number (CAS No.) 64379-44-8, is a significant heterocyclic compound that has garnered considerable attention in the field of pharmaceutical chemistry and medicinal research. This compound belongs to the naphthyridine class, a nitrogen-containing heterocycle that exhibits a broad spectrum of biological activities, making it a valuable scaffold for drug discovery and development.
The structural framework of 1,5-naphthyridine-4-carbaldehyde consists of two fused pyridine rings, with a carbonyl group positioned at the 4-position. This specific arrangement imparts unique electronic and steric properties to the molecule, which are exploited in various synthetic and pharmacological applications. The presence of the aldehyde functionality further enhances its reactivity, enabling diverse chemical transformations that are pivotal in medicinal chemistry.
In recent years, 1,5-naphthyridine-4-carbaldehyde has been extensively studied for its potential in developing novel therapeutic agents. Its core structure is reminiscent of several bioactive molecules that have shown efficacy in treating a range of diseases, including cancer, infectious diseases, and inflammatory disorders. The naphthyridine scaffold is particularly noted for its ability to interact with biological targets such as enzymes and receptors, thereby modulating cellular processes.
One of the most compelling aspects of 1,5-naphthyridine-4-carbaldehyde is its role as a key intermediate in synthesizing more complex pharmacophores. Researchers have leveraged its reactive aldehyde group to form Schiff bases, hydrazones, and other derivatives that exhibit enhanced biological activity. For instance, studies have demonstrated that derivatives of this compound can inhibit specific enzymes involved in cancer progression by binding to their active sites and disrupting their function.
Recent advancements in computational chemistry have also highlighted the importance of 1,5-naphthyridine-4-carbaldehyde in virtual screening campaigns. High-throughput docking simulations have identified potential lead compounds derived from this scaffold that show promise against various therapeutic targets. These computational approaches have significantly accelerated the drug discovery process by allowing researchers to predict binding affinities and optimize molecular structures before conducting wet-lab experiments.
The pharmaceutical industry has been particularly interested in exploring the antimicrobial properties of compounds derived from 1,5-naphthyridine-4-carbaldehyde. Emerging evidence suggests that certain derivatives exhibit potent activity against multidrug-resistant bacteria, offering a much-needed solution to the growing threat of antibiotic resistance. This has spurred further research into developing novel antibiotics based on this structural motif.
Moreover, 1,5-naphthyridine-4-carbaldehyde has found applications in materials science due to its ability to form coordination complexes with metal ions. These complexes have been investigated for their catalytic properties and potential use in industrial processes. The versatility of this compound underscores its importance not only in drug development but also in broader chemical applications.
The synthesis of 1,5-naphthyridine-4-carbaldehyde itself is a topic of considerable interest among synthetic chemists. Various methodologies have been developed to construct the naphthyridine core efficiently while introducing functional groups at specific positions. One notable approach involves condensation reactions between appropriate precursors followed by oxidation to introduce the aldehyde functionality. These synthetic strategies are continuously being refined to improve yield and scalability.
In conclusion, 1,5-naphthyridine-4-carbaldehyde (CAS No. 64379-44-8) represents a structurally intriguing and biologically relevant compound with far-reaching implications in pharmaceutical research and industrial chemistry. Its unique properties make it an invaluable building block for developing new drugs and materials, and ongoing studies continue to uncover its full potential across multiple disciplines.
64379-44-8 (1,5-naphthyridine-4-carbaldehyde) Related Products
- 179381-15-8(Pyrrolo[1,2-a]pyrazine-8-carbaldehyde)
- 132911-52-5(12H-Indolo[2',3':3,4]pyrido[1,2-a]indole-13-carboxaldehyde)
- 25957-65-7(1H-Pyrrolo[2,3-c]pyridine-3-carbaldehyde)
- 56671-64-8(Indolizine-1-carbaldehyde)
- 885278-16-0(1,6-naphthyridine-8-carbaldehyde)
- 141234-08-4(Quinoxaline-5-carbaldehyde)
- 1020056-33-0(1H-Pyrrolo3,2-bpyridine-6-carbaldehyde)
- 38707-70-9(quinoline-8-carbaldehyde)
- 276862-85-2(1H-Pyrrolo[3,2-b]pyridine-3-carbaldehyde)
- 79426-14-5(1,5-Naphthyridine-4-carboxylic acid)