≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Exo-5-norbornenecarboxylic acid is a bicyclic compound that has potential applications in the field of material science due to its unique chemical properties. It is a versatile building block for the synthesis of various functional materials, including polymers, dendrimers, and self-assembled monolayers. It can be used to modify surfaces or to functionalize nanoparticles, influencing their optical, magnetic, or electronic properties. It is also often used in ring-opening metathesis polymerization reactions to form polymers with controlled molecular weight and structure. Additionally, exo-5-norbornenecarboxylic acid can function as a ligand for coordination chemistry and catalysis.
Product Application:
Exo-5-norbornenecarboxylic acid can be used as:
A starting material in the synthesis of the metathesis polymer via a ring-opening metathesis polymerization (ROMP) reaction of the ester of exo-5-norbornenecarboxylic acid and 1,1′-bi-2-naphthol.
A monomer in the preparation of thin films via surface-initiated polymerization process. The resulting thin film serves as a template for selective deposition and etching of metal oxides, which is of significant importance in the microelectronic industry.
exo-5-Norbornenecarboxylic acid can be used as a precursor in the synthesis of:
Different crosslinkers for ring-opening metathesis polymerization.
Norbornene-functionalized monomers, which are used to make poly(norbornene)s via ring-opening metathesis polymerization (ROMP).
Hydrolytically cleavable and hydrolytically stable functionalized macromonomers for hydrogel preparation.
| Pubchem Sid | 504767025 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504767025 |
| Sonrisas canónicas | C1C2CC(C1C=C2)C(=O)O |
| IUPAC Name | (1R,2S,4R)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid |
| InChIKey | FYGUSUBEMUKACF-VQVTYTSYSA-N |
| INCHI | 1S/C8H10O2/c9-8(10)7-4-5-1-2-6(7)3-5/h1-2,5-7H,3-4H2,(H,9,10)/t5-,6+,7+/m1/s1 |
| Isómeros SMILES | C1[C@@H]2C[C@@H]([C@H]1C=C2)C(=O)O |
| Peso molecular | 138.16 |
| Reaxy-Rn | 4662674 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4662674&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | Carboxylic acids and derivatives |
| Subclass | Carboxylic acids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Carboxylic acids |
| Alternative Parents | Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 F2330563 | Certificate of Analysis | Apr 03, 2026 | E469877 |
| F2330578 | Certificate of Analysis | Apr 03, 2026 | E469877 |
| A2622403 | Certificate of Analysis | Jan 12, 2026 | E469877 |
| A2622424 | Certificate of Analysis | Jan 12, 2026 | E469877 |
| D2501265 | Certificate of Analysis | Mar 22, 2025 | E469877 |
| D2501280 | Certificate of Analysis | Mar 22, 2025 | E469877 |
| H2507149 | Certificate of Analysis | Mar 22, 2025 | E469877 |
| K2528084 | Certificate of Analysis | Mar 22, 2025 | E469877 |
| E2420206 | Certificate of Analysis | May 08, 2024 | E469877 |
| E2420208 | Certificate of Analysis | May 08, 2024 | E469877 |
| F2330573 | Certificate of Analysis | Jun 05, 2023 | E469877 |
| F2330577 | Certificate of Analysis | Jun 05, 2023 | E469877 |
| Índice de refracción | n20/D 1.494 |
|---|---|
| Punto de inflamación (°F) | 230.0 °F |
| Punto de inflamación (°C) | > 110 °C |
| Punto de ebullición (°C) | 136-138 °C/14 mmHg (lit.) |
| Punto de fusión (°C) | 40-44℃ |
| Peso molecular | 138.160 g/mol |
| XLogP3 | 1.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 138.068 Da |
| Monoisotopic Mass | 138.068 Da |
| Topological Polar Surface Area | 37.300 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 195.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
