Cas no 1262435-15-3 (sodium bicyclo[2.2.1]heptane-2-carboxylate)
sodium bicyclo[2.2.1]heptane-2-carboxylate Chemical and Physical Properties
Names and Identifiers
-
- sodium bicyclo[2.2.1]heptane-2-carboxylate
- Sodiumbicyclo[221]heptane-2-carboxylate
- sodium (1R,2S,4S)-bicyclo[2.2.1]heptane-2-carboxylate
- 1262435-15-3
- sodium;bicyclo[2.2.1]heptane-2-carboxylate
- SCHEMBL3854942
- sodium (1R,4S)-bicyclo[2.2.1]heptane-2-carboxylate
- Sodium bicyclo[2,2,1]heptane-2-carboxylate
-
- MDL: MFCD28964176
- Inchi: 1S/C8H12O2.Na/c9-8(10)7-4-5-1-2-6(7)3-5;/h5-7H,1-4H2,(H,9,10);/q;+1/p-1
- InChI Key: WVHYWHGOIJEBAT-UHFFFAOYSA-M
- SMILES: [Na+].[O-]C(C1CC2CCC1C2)=O
Computed Properties
- Exact Mass: 162.06567387Da
- Monoisotopic Mass: 162.06567387Da
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 11
- Rotatable Bond Count: 1
- Complexity: 169
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 3
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 40.1?2
sodium bicyclo[2.2.1]heptane-2-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A450001380-1g |
Sodium bicyclo[2.2.1]heptane-2-carboxylate |
1262435-15-3 | 97% | 1g |
507.18 USD | 2021-06-11 | |
| Alichem | A450001380-5g |
Sodium bicyclo[2.2.1]heptane-2-carboxylate |
1262435-15-3 | 97% | 5g |
1,421.00 USD | 2021-06-11 | |
| abcr | AB459495-250 mg |
Sodium bicyclo[2.2.1]heptane-2-carboxylate |
1262435-15-3 | 250mg |
€354.60 | 2023-04-22 | ||
| abcr | AB459495-1 g |
Sodium bicyclo[2.2.1]heptane-2-carboxylate |
1262435-15-3 | 1g |
€804.70 | 2023-04-22 | ||
| Chemenu | CM322198-1g |
sodium (1R,4S)-bicyclo[2.2.1]heptane-2-carboxylate |
1262435-15-3 | 95% | 1g |
$524 | 2023-03-07 | |
| Chemenu | CM322198-1g |
sodium (1R,4S)-bicyclo[2.2.1]heptane-2-carboxylate |
1262435-15-3 | 95% | 1g |
$524 | 2021-06-15 | |
| abcr | AB459495-250mg |
Sodium bicyclo[2.2.1]heptane-2-carboxylate; . |
1262435-15-3 | 250mg |
€375.70 | 2025-04-21 | ||
| abcr | AB459495-1g |
Sodium bicyclo[2.2.1]heptane-2-carboxylate; . |
1262435-15-3 | 1g |
€857.10 | 2025-04-21 | ||
| 1PlusChem | 1P00HRW8-250mg |
Sodiumbicyclo[221]heptane-2-carboxylate |
1262435-15-3 | 97% | 250mg |
$247.00 | 2024-07-09 | |
| Ambeed | A101293-1g |
exo-Sodium bicyclo[2.2.1]heptane-2-carboxylate |
1262435-15-3 | 95+% | 1g |
$469.0 | 2024-04-25 |
sodium bicyclo[2.2.1]heptane-2-carboxylate Related Literature
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Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
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Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa Caccamo Phys. Chem. Chem. Phys., 2019,21, 11983-11991
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
Additional information on sodium bicyclo[2.2.1]heptane-2-carboxylate
Exploring Sodium Bicyclo[2.2.1]heptane-2-carboxylate (CAS No. 1262435-15-3): Properties, Applications, and Innovations
Sodium bicyclo[2.2.1]heptane-2-carboxylate (CAS No. 1262435-15-3) is a specialized organic compound gaining attention in pharmaceutical and chemical research due to its unique bicyclic structure. The bicyclo[2.2.1]heptane (norbornane) framework, combined with a carboxylate group, offers exceptional steric and electronic properties, making it valuable for drug design, catalysis, and material science. Researchers are increasingly exploring its potential as a chiral building block or ligand precursor in asymmetric synthesis, aligning with the growing demand for enantioselective methodologies.
In recent years, the compound’s water-soluble sodium salt form has become a focal point for applications requiring improved bioavailability or environmental compatibility. Its stability under physiological conditions makes it a candidate for prodrug development, a hot topic in biopharmaceutical innovation. Notably, the rise of green chemistry has spurred interest in derivatives like sodium bicyclo[2.2.1]heptane-2-carboxylate as eco-friendly alternatives in industrial processes, addressing concerns about solvent waste and toxicity.
The compound’s CAS No. 1262435-15-3 is frequently searched in academic and patent databases, reflecting its relevance in intellectual property (IP) landscapes. Startups and R&D teams are investigating its role in high-value fine chemicals, particularly for neuroactive drug intermediates, where rigid bicyclic structures enhance target selectivity. This aligns with trends in central nervous system (CNS) drug discovery, a sector experiencing rapid growth due to unmet medical needs.
From a synthetic perspective, the bicyclo[2.2.1]heptane core provides a platform for structural diversification. Chemists leverage its strain energy to facilitate ring-opening reactions or cascade cyclizations, topics trending in methodology papers and AI-assisted retrosynthesis tools. Computational studies on this compound often appear in discussions about molecular docking and 3D pharmacophore modeling, highlighting its interdisciplinary appeal.
In material science, the sodium salt’s anionic surfactant-like behavior is under scrutiny for nanoparticle stabilization or polymeric matrix modification. Such applications resonate with the booming nanotechnology sector, where search queries for “functionalized bicyclic additives” have surged. Additionally, its potential in biodegradable chelators taps into the global push for sustainable alternatives to EDTA derivatives.
Quality control of CAS 1262435-15-3 remains critical, with analytical techniques like HPLC-MS and NMR purity profiling being common search terms among purchasers. Suppliers emphasizing GMP-grade synthesis or low heavy-metal specifications cater to the stringent requirements of clinical-stage developers, a niche with expanding market demand.
Looking ahead, the intersection of sodium bicyclo[2.2.1]heptane-2-carboxylate with machine learning in chemistry presents untapped opportunities. Predictive algorithms could optimize its use in combinatorial libraries or catalytic systems, addressing frequent queries about “next-gen bicyclic platforms.” As regulatory landscapes evolve, this compound’s REACH compliance and toxicological profiles will likely dominate industry discussions, ensuring its place in future innovations.
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