Direkt zum Inhalt
Merck
Alle Fotos(2)

Key Documents

View All Documentation

718149

Sigma-Aldrich

exo-5-Norbornen-Carboxylsäure

97%

Synonym(e):

(1R,2S,4R)-Bicyclo[2.2.1]hept-5-en-2-carbonsäure, NC

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(2)

About This Item

Empirische Formel (Hill-System):
C8H10O2
CAS-Nummer:
934-30-5
Molekulargewicht:
138.16
MDL-Nummer:
MFCD00213362
UNSPSC-Code:
12162002
PubChem Substanz-ID:
329763554
NACRES:
NA.23

Assay

97%

Form

solid

mp (Schmelzpunkt)

40-44 °C

SMILES String

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

InChIKey

FYGUSUBEMUKACF-RRKCRQDMSA-N

Allgemeine Beschreibung

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.

Anwendung

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.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

>230.0 °F

Flammpunkt (°C)

> 110 °C

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCQ4334
MKCP2222
MKCN9698
MKCN9699
MKCN3067

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Suche nach COA

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Kunden haben sich ebenfalls angesehen

Slide 1 of 2

1 of 2

2-Norbornanmethanol, Mischung aus endo und exo 97%

Sigma-Aldrich

109398

2-Norbornanmethanol, Mischung aus endo und exo

1-Cyclohexen-1-carbonsäure 97%

Sigma-Aldrich

328367

1-Cyclohexen-1-carbonsäure

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
Nilwala Kottegoda et al.
ACS nano, 11(2), 1214-1221 (2017-01-26)
While slow release of chemicals has been widely applied for drug delivery, little work has been done on using this general nanotechnology-based principle for delivering nutrients to crops. In developing countries, the cost of fertilizers can be significant and is
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
Manuel Gregoritza et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 127, 194-203 (2018-02-23)
Reducing burst effects, providing controlled release, and safeguarding biologics against degradation are a few of several highly attractive applications for microgels in the field of controlled release. However, the incorporation of proteins into microgels without impairing stability is highly challenging.
Alle zugehörigen Dokumente anzeigen

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.