182250-70-0

Basic information

• Product Name: 3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL
• Synonyms: 3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL;Bisbutyldiphenylsilyloxybenzylalcohol;3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL 95+%;3,5-Bis(tert-butyldiphenylsilyloxy)benzyl Alcohol;(3,5-Bis((tert-butyldiphenylsilyl)
• CAS NO: 182250-70-0
• Molecular Formula: C₃₉H₄₄O₃Si₂
• Molecular Weight: 616.94
• Product Categories: Building Blocks for Dendrimers;Functional Materials;Monoalkoxysilanes;Si (Classes of Silicon Compounds);Si-O Compounds
• Mol File: 182250-70-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 108 °C
• Boiling Point: 631.648oC at 760 mmHg
• Flash Point: 335.809oC
• Appearance: /
• Density: 1.116g/cm3
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.603
• CAS DataBase Reference: 3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL(182250-70-0)
• EPA Substance Registry System: 3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL(182250-70-0)

Safety Data

• Hazardous Substances Data: 182250-70-0(Hazardous Substances Data)

Usage

General Description

3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL is a chemical compound with the molecular formula C56H62O2Si2. It is a benzyl alcohol derivative that contains tert-butyl and diphenylsilyloxy groups. 3,5-BIS(TERT-BUTYLDIPHENYLSILYLOXY)BENZYL ALCOHOL is used in organic synthesis and pharmaceutical research as a versatile building block for the preparation of various functional organic compounds. It has been found to exhibit potential biological activities and has applications in drug discovery and development. Additionally, due to its unique structure, it also has potential use in materials science and nanotechnology.

InChI:InChI=1/C39H44O3Si2/c1-38(2,3)43(34-19-11-7-12-20-34,35-21-13-8-14-22-35)41-32-27-31(30-40)28-33(29-32)42-44(39(4,5)6,36-23-15-9-16-24-36)37-25-17-10-18-26-37/h7-29,40H,30H2,1-6H3

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 182250-68-6 methyl 3,5-bis(tert-butyldiphenylsilyloxy)benzoate 

Downstream Products

• 150551-00-1 3,5-bis(3,5-bis(4-methoxycarbonylphenyl)benzyloxy)benzyl alcohol 
• 636984-69-5 3,5-dibromo[3',5'-bis(tert-butyldiphenylsiloxy)benzyloxy]benzene 

Relevant articles and documents

A simple method for controlling dendritic architecture and diversity: A parallel monomer combination approach

A novel parallel monomer combination approach to manipulating the architectural disposition of dendritic macromolecules is described. It harnesses the synthetic speed and power of the double-stage convergent growth approach and classical parallel synthesi

A fast double-stage convergent synthesis of dendritic polyethers

Two tert-butyldiphenylsilyl-protected synthons 7 and 9 are prepared in excellent yields and used in a one-pot synthesis of higher generation polyether dendrons.