exo-5-Norbornenecarboxylic acid - ≥97% , CAS No.934-30-5

CAS: 934-30-5 Cat. No.: E469877 Summenformel: C₈H₁₀O₂ Molekulargewicht: 138.16 EG-Nummer: 624-387-6

GRADE & PURITY ≥97%

Synonyms

rac-(1R,2S,4R)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid | Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, (1R,2S,4R)-rel- | exo-5-Norbornenecarboxylic acid | MFCD08899816 | SCHEMBL900095 | (1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid

Storage

Store at 2-8°C

Shipped In

Wet ice

Übersicht

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.

Specifications

Synonyme

rac-(1R,2S,4R)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid | Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, (1R,2S,4R)-rel- | exo-5-Norbornenecarboxylic acid | MFCD08899816 | SCHEMBL900095 | (1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid

Spezifikationen & Reinheit

≥97%

Storage

Store at 2-8°C

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥97%

Namen und Kennungen

Pubchem Sid

504767025

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504767025

Kanonisches Lächeln

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

Isomere SMILES

C1[C@@H]2C[C@@H]([C@H]1C=C2)C(=O)O

Molekulargewicht

138.16

Reaxy-Rn

4662674

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4662674&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: 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
• Beschreibung: 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

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemische und physikalische Eigenschaften

• Brechungsindex: n20/D 1.494
• Flammpunkt (°F): 230.0 °F
• Flammpunkt (°C): > 110 °C
• Siedepunkt (°C): 136-138 °C/14 mmHg (lit.)
• Schmelzpunkt (°C): 40-44℃
• Molekulargewicht: 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