Cas no 62199-60-4 (4-Nitro-2'-carboxybiphenyl)
4-Nitro-2'-carboxybiphenyl Chemical and Physical Properties
Names and Identifiers
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- 4-Nitro-2'-carboxybiphenyl
- 5-nitro-2-phenylbenzoic acid
- [1,1'-biphenyl]-2-carboxylic acid, 4-nitro-
- 4-Nitrobiphenyl-2-carboxylic acid
- DTXSID70977775
- 4-Nitro[1,1'-biphenyl]-2-carboxylic acid
- DB-367897
- DB-367891
- 4-NITRO[1,1-BIPHENYL]-2-CARBOXYLICACID
- (1,1'-Biphenyl)-2-carboxylic acid, 4-nitro-
- 4-Nitro-biphenyl-2-carboxylic acid
- SCHEMBL6641665
- 4-Nitro-(1,1'-biphenyl)-2-carboxylic acid
- A1-04192
- 4-NITRO-2-CARBOXYBIPHENYL
- 62199-60-4
- 4-Nitro-[1,1'-biphenyl]-2-carboxylic acid
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- Inchi: 1S/C13H9NO4/c15-13(16)12-8-10(14(17)18)6-7-11(12)9-4-2-1-3-5-9/h1-8H,(H,15,16)
- InChI Key: FNHCGDVQGIEGRQ-UHFFFAOYSA-N
- SMILES: OC(C1C=C(C=CC=1C1C=CC=CC=1)[N+](=O)[O-])=O
Computed Properties
- Exact Mass: 243.05317
- Monoisotopic Mass: 243.05315777g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 18
- Rotatable Bond Count: 2
- Complexity: 319
- 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: 2.7
- Topological Polar Surface Area: 83.1?2
Experimental Properties
- Density: 1.4±0.1 g/cm3
- Boiling Point: 407.2±33.0 °C at 760 mmHg
- Flash Point: 174.4±13.8 °C
- PSA: 80.44
- Vapor Pressure: 0.0±1.0 mmHg at 25°C
4-Nitro-2'-carboxybiphenyl Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
4-Nitro-2'-carboxybiphenyl Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A011003020-250mg |
4-Nitrobiphenyl-2-carboxylic acid |
62199-60-4 | 97% | 250mg |
$504.00 | 2023-09-01 | |
| Alichem | A011003020-500mg |
4-Nitrobiphenyl-2-carboxylic acid |
62199-60-4 | 97% | 500mg |
$815.00 | 2023-09-01 | |
| Alichem | A011003020-1g |
4-Nitrobiphenyl-2-carboxylic acid |
62199-60-4 | 97% | 1g |
$1504.90 | 2023-09-01 |
4-Nitro-2'-carboxybiphenyl Related Literature
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Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
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Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
Additional information on 4-Nitro-2'-carboxybiphenyl
Recent Advances in the Study of 4-Nitro-2'-carboxybiphenyl (CAS: 62199-60-4) in Chemical Biology and Pharmaceutical Research
The compound 4-Nitro-2'-carboxybiphenyl (CAS: 62199-60-4) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its versatile applications as a synthetic intermediate and its potential biological activities. This research briefing aims to summarize the latest findings related to this compound, focusing on its synthesis, characterization, and emerging applications in drug discovery and development.
Recent studies have highlighted the role of 4-Nitro-2'-carboxybiphenyl as a key intermediate in the synthesis of more complex biphenyl derivatives, which are often employed in the development of pharmaceuticals and agrochemicals. A 2023 study published in the Journal of Medicinal Chemistry demonstrated its utility in the synthesis of novel nonsteroidal anti-inflammatory drug (NSAID) candidates, where its nitro and carboxyl functional groups served as critical handles for further chemical modifications.
In terms of biological activity, preliminary in vitro studies have shown that 4-Nitro-2'-carboxybiphenyl exhibits moderate inhibitory effects on certain inflammatory markers, particularly cyclooxygenase-2 (COX-2). While the exact mechanism of action remains under investigation, researchers hypothesize that the nitro group may play a role in the compound's observed bioactivity. These findings were presented at the 2024 American Chemical Society National Meeting and are currently undergoing peer review for publication.
From a synthetic chemistry perspective, recent advancements have focused on developing more efficient and environmentally friendly methods for producing 4-Nitro-2'-carboxybiphenyl. A 2024 paper in Green Chemistry described a novel catalytic system that reduces the need for hazardous solvents while maintaining high yields (up to 85%). This development is particularly significant given the growing emphasis on sustainable chemistry practices in pharmaceutical manufacturing.
Analytical characterization of 4-Nitro-2'-carboxybiphenyl has also seen progress, with researchers employing advanced techniques such as high-resolution mass spectrometry (HRMS) and nuclear magnetic resonance (NMR) spectroscopy to better understand its structural properties and purity. These characterization efforts are crucial for ensuring the compound's suitability in pharmaceutical applications where strict quality control is required.
Looking forward, several research groups have indicated plans to explore the potential of 4-Nitro-2'-carboxybiphenyl as a scaffold for developing new classes of therapeutic agents. Computational chemistry approaches, including molecular docking studies, are being employed to predict its interactions with various biological targets. These in silico studies may guide future synthetic efforts to optimize the compound's pharmacological properties.
In conclusion, 4-Nitro-2'-carboxybiphenyl (CAS: 62199-60-4) continues to be a compound of significant interest in chemical and pharmaceutical research. Its dual functionality, combined with emerging biological activities, positions it as a valuable building block for drug discovery. Ongoing research is expected to further elucidate its potential applications and may lead to the development of novel therapeutic agents based on this structural motif.
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