934550

Silyl-ether based ROMP monomer

iPrSi

• Synonyme(s) : 2,2-Bis(1-methylethyl)-1,3-dioxa-2-silacyclohept-5-ene
• Formule empirique (notation de Hill): C₁₁H₂₂O₂Si
• Numéro CAS: 2396521-63-2
• Poids moléculaire : 214.38
• Numéro MDL: MFCD34470659
• Code UNSPSC : 12162002
• Nomenclature NACRES : NA.21

Propriétés

• Essai: ≥98%
• Niveau de qualité: 100
• Forme: liquid
• Composition: iPrSi
• Couleur: colorless to pale yellow
• Température de stockage: 2-8°C
• Chaîne SMILES: CC(C)[Si]1(C(C)C)OC/C=C\CCO1
• InChI: 1S/C11H22O2Si/c1-10(2)14(11(3)4)12-8-6-5-7-9-13-14/h5-6,10-11H,7-9H2,1-4H3/b6-5-
• Clé InChI: YBYQYMPJHKPHMH-WAYWQWQTSA-N

Description

Description générale

Ring opening metathesis polymerization (ROMP) monomers are attractive building block for advanced polymeric materials in the biomedical field. 2,2-Bis(1-methylethyl)-1,3-dioxa-2-silacyclohept-5-ene , or the silyl ether based ROMP monomer iPrSi, is a bifunctional cyclic olefin that can be used to synthesize a variety of marcomolecules and polymers with diverse compositions and complex structures. iPrSi can copolymerize with a variety of norbornene derivatives including small molecules and macromolecules, enabling the formation of backbone-degradable copolymers that can be used in a variety of biomedical applications. The ROMP polymerization method is superior as it permits the tailorability of the resulting polymer material.

Application

Synthesis of advanced polymeric materials for biomedical applications including:

• drug delivery
• molecular imaging
• self assembly
• hydrogels
• medical device coatings
• stimuli responsive material

Caractéristiques et avantages

• Copolymerize efficiency with a wide variety of norbornene-based (macro)monomers
• Controlled ROMP polymerization
• Silyl ether substitute can be tuned to control degradation

Informations sur la sécurité

• Code de la classe de stockage: 10 - Combustible liquids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable