4115-83-7

Basic information

• Product Name: POLY(CYCLOHEXYLSILSESQUIOXANE) SILANOL FUNCTIONAL
• Synonyms: POLY(CYCLOHEXYLSILSESQUIOXANE) SILANOL FUNCTIONAL;POLY(CYCLOHEXYLSILSESQUIOXANE): SILANOL FUNCTIONAL, 5.1-5.4% OH;POLY(CYCLOHEXYLSILSESQUIOXANE);SILANOL FUNCTIONAL, 5.1-5.4% OH
• CAS NO: 4115-83-7
• Molecular Formula: C42H80O12Si7
• Molecular Weight: 973.6759
• Mol File: 4115-83-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: POLY(CYCLOHEXYLSILSESQUIOXANE) SILANOL FUNCTIONAL(CAS DataBase Reference)
• NIST Chemistry Reference: POLY(CYCLOHEXYLSILSESQUIOXANE) SILANOL FUNCTIONAL(4115-83-7)
• EPA Substance Registry System: POLY(CYCLOHEXYLSILSESQUIOXANE) SILANOL FUNCTIONAL(4115-83-7)

Safety Data

• Hazardous Substances Data: 4115-83-7(Hazardous Substances Data)

Upstream product

• 98-12-4 cyclohexyltrichlorosilane 
• 3553-72-8 hexacyclohexyl-hexasilsesquioxane 
• 110-83-8 cyclohexene 

Downstream Products

• 132297-51-9 Si₇BiO₁₂(c-C₆H₁₁)7 
• 288300-61-8 Yb⁽³⁺⁾*(C₆H₁₁)7Si₇O₁₂^(3-)*CH₃N(CH₂CH₂N(CH₃)2)2=((C₆H₁₁)7Si₇O₁₂)Yb(CH₃N(CH₂CH₂N(CH₃)2)2) 
• 133323-69-0 (c-C₆H₁₁)7Si₇O₁₂V(O) 
• 255839-46-4 Ti(OC₆H₅)((C₆H₁₁)7Si₇O₁₂) 
• 255839-50-0 Ti(OC₆H₄F)((C₆H₁₁)7Si₇O₁₂) 
• 193274-05-4 Ti(OC₆H₄NO₂)((C₆H₁₁)7Si₇O₁₂) 

Relevant articles and documents

Facile and remarkably selective substitution reactions involving framework silicon atoms in silsesquioxane frameworks

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A new route to incompletely-condensed silsesquioxanes: Base-mediated cleavage of polyhedral oligosilsesquioxanes

Readily available R8Si8O12 frameworks react selectively with aqueous Et4NOH to afford discrete incompletely-condensed silsesquioxanes: reaction of R8Si8O12 (2a, R = c-C6/su

Silsesquioxanes as Models for Silica Surfaces

The hydrolytic condensation of cyclohexyltrichlorosilane (CySiCl3) affords (1), (2), and (3a).Trisilanol 1 and 3b, the bis(triphenyltin) derivative of 3a, have been structurally characterized by single-crystal X-ray diffraction studies.Trisilanol 1 undergoes corner-capping reactions with trifunctional monomers (e.g., R'SiCl3, MeGeCl3, MeSnCl3), is selectively monosilylated to (6a) with chlorotrimethylsilane, and can be dehydrated to (7a).Comparison of the molecular structure of 1 with (111) β-cristobalite and (0001)β-tridymite reveals many structural similarities.Silsesquioxanes 1, 6a, and 7a are discussed as models for silica surfaces.