Accéder au contenu
Merck
Toutes les photos(2)

Key Documents

View All Documentation

718149

Sigma-Aldrich

exo-5-Norbornenecarboxylic acid

97%

Synonyme(s) :

(1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, NC

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(2)

About This Item

Formule empirique (notation de Hill):
C8H10O2
Numéro CAS:
934-30-5
Poids moléculaire :
138.16
Numéro MDL:
MFCD00213362
Code UNSPSC :
12162002
ID de substance PubChem :
329763554
Nomenclature NACRES :
NA.23

Niveau de qualité

100

Pureté

97%

Forme

solid

Pf

40-44 °C

Chaîne SMILES 

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

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+/m0/s1

Clé InChI

FYGUSUBEMUKACF-RRKCRQDMSA-N

Description générale

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.

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.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

>230.0 °F

Point d'éclair (°C)

> 110 °C

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
MKCV6892
MKCT2690
MKCT7799
MKCQ8721
MKCQ1232

Vous ne trouvez pas la bonne version ?

Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

Rechercher un(e) COA

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Les clients ont également consulté

Slide 1 of 2

1 of 2

2-Norbornanemethanol, mixture of endo and exo 97%

Sigma-Aldrich

109398

2-Norbornanemethanol, mixture of endo and exo

1-Cyclohexene-1-carboxylic acid 97%

Sigma-Aldrich

328367

1-Cyclohexene-1-carboxylic acid

Jürgen Herrler et al.
Magnetic resonance in medicine, 85(6), 3140-3153 (2021-01-06)
To mitigate spatial flip angle (FA) variations under strict specific absorption rate (SAR) constraints for ultra-high field MRI using a combination of universal parallel transmit (pTx) pulses and fast subject-specific optimization. Data sets consisting of B0 , B 1 +
Wenjun Zheng et al.
BMC structural biology, 9, 45-45 (2009-07-14)
It is increasingly recognized that protein functions often require intricate conformational dynamics, which involves a network of key amino acid residues that couple spatially separated functional sites. Tremendous efforts have been made to identify these key residues by experimental and
Christopher L McGann et al.
Macromolecular bioscience, 16(1), 129-138 (2015-10-06)
A range of chemical strategies have been used for crosslinking recombinant polypeptide hydrogels, although only a few have employed photocrosslinking approaches. Here, we capitalize on the novel insect protein, resilin, and the versatility of click reactions to introduce a resilin-like
Patricia Gumbley et al.
Macromolecular rapid communications, 34(23-24), 1838-1843 (2013-11-12)
This communication describes photoresponsive gels, prepared using ring-opening metathesis polymerization (ROMP), that dissolve upon irradiation with ultraviolet light. Exposure of mixtures of norbornene-type ROMP monomers and new photoreactive cross-linkers comprising two norbornene units bound through a chain containing o-nitrobenzyl esters
Stefano Longhi et al.
Optics letters, 45(7), 1962-1965 (2020-04-03)
Multimode interference (MMI) and self-imaging are important phenomena of diffractive optics with major applications in signal processing, beam shaping, and optical sensing. Such phenomena generally arise from interference of normal modes in lossless dielectric guiding structures; however, the impact of
Afficher tous les articles scientifiques apparentés

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique