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1,5-Trisiloxanediol, 1,1,3,3,5,5-hexaphenyl- is a complex organic compound with the chemical formula C36H30O3Si3. It is a cyclic siloxane molecule consisting of three silicon atoms connected to three oxygen atoms, forming a six-membered ring. The hexaphenyl substituents are attached to the silicon atoms, with each phenyl group containing six carbon atoms. 1,5-Trisiloxanediol, 1,1,3,3,5,5-hexaphenyl- is characterized by its unique structure and properties, making it useful in various applications such as in the synthesis of silicone-based materials, as a precursor in the production of specialty chemicals, and potentially in the development of new materials with specific optical, electronic, or mechanical properties. Due to its complex structure, it is typically synthesized through multi-step processes and is of interest to researchers in the field of organosilicon chemistry.

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  • 1110-85-6 Structure
  • Basic information

    1. Product Name: 1,5-Trisiloxanediol, 1,1,3,3,5,5-hexaphenyl-
    2. Synonyms:
    3. CAS NO:1110-85-6
    4. Molecular Formula: C36H32O4Si3
    5. Molecular Weight: 612.904
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1110-85-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,5-Trisiloxanediol, 1,1,3,3,5,5-hexaphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,5-Trisiloxanediol, 1,1,3,3,5,5-hexaphenyl-(1110-85-6)
    11. EPA Substance Registry System: 1,5-Trisiloxanediol, 1,1,3,3,5,5-hexaphenyl-(1110-85-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1110-85-6(Hazardous Substances Data)

1110-85-6 Usage

Chemical Structure

A 1,5-trisiloxane backbone with three hydroxyl groups and six phenyl groups attached to the silicon atoms.

Type of Compound

A type of siloxane, which is a group of silicon-oxygen compounds.

Commonly Found In

Silicone polymers.

Unique Properties

Presence of phenyl groups in the molecule.

Industrial Applications

Useful in the production of silicone-based materials, lubricants, and coatings.

Chemical Reactivity

Hydroxyl groups in the compound's structure enable it to participate in various chemical reactions.

Versatility

Potential for use in a wide range of applications due to its unique properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1110-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1110-85:
(6*1)+(5*1)+(4*1)+(3*0)+(2*8)+(1*5)=36
36 % 10 = 6
So 1110-85-6 is a valid CAS Registry Number.

1110-85-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-dihydroxyhexaphenyltrisiloxane

1.2 Other means of identification

Product number -
Other names .1,1,3,3,5,5-hexaphenyl-1,3,5-trisiloxane-1,5-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1110-85-6 SDS

1110-85-6Relevant articles and documents

The structure of 1,1,3,3,5,5-hexaphenyl-1,3,5-trisiloxane-1,5-diol

Behbehani, H.,Brisdon, B. J.,Mahon, M. F.,Molloy, K. C.,Mazhar, M.

, p. 41 - 46 (2007/10/02)

1,1,3,3,5,5-Hexaphenyl-1,3,5-trisiloxane-1,5-diol has an approximately planar, eight-membered Si3O4H ring structure, in which cyclization is achieved through an O-H...O hydrogen bond.In addition, adjacent molecules dimerize through an eight-membered H4O4 ring to yield a stepped tricyclic array.

Metallkomplexe in Anorganichen Matrices, 5. Katalytische Silanoxidation an einem heterogenisierten Rhodium-Komplex

Egger, Christian,Schubert, Ulrich

, p. 783 - 788 (2007/10/02)

A heterogenized rhodium complex, prepared by sol-gel processing of Rh(CO)Cl2 and Si(OEt)4, is shown to catalyze the conversion of the silanes H4-nSiPhn (n = 1-3) or (HMe2Si)2O to (poly)siloxanes by air or water.Using THF as a solvent, the silanoles Ph3SiOH or Ph2Si(OH)2 are obtained instead.The reaction of phenylacetic acid or acetic acid with HSiPh3 to give silyl esters is catalyzed by the same compound.

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