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Phenol, 4-bromo-2-(trimethylsilyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67044-81-9 Structure
  • Basic information

    1. Product Name: Phenol, 4-bromo-2-(trimethylsilyl)-
    2. Synonyms:
    3. CAS NO:67044-81-9
    4. Molecular Formula: C9H13BrOSi
    5. Molecular Weight: 245.191
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67044-81-9.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: Phenol, 4-bromo-2-(trimethylsilyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 4-bromo-2-(trimethylsilyl)-(67044-81-9)
    11. EPA Substance Registry System: Phenol, 4-bromo-2-(trimethylsilyl)-(67044-81-9)
  • 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: 67044-81-9(Hazardous Substances Data)

67044-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67044-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,4 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67044-81:
(7*6)+(6*7)+(5*0)+(4*4)+(3*4)+(2*8)+(1*1)=129
129 % 10 = 9
So 67044-81-9 is a valid CAS Registry Number.

67044-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-2-trimethylsilanyl-phenol

1.2 Other means of identification

Product number -
Other names (2-Hydroxy-5-brom-penyl)-trimethylsilan

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:67044-81-9 SDS

67044-81-9Relevant articles and documents

Lowerature Cross-Linking Benzocyclobutene Based Polymer Dielectric for Organic Thin Film Transistors on Plastic Substrates

Hallani, Rawad K.,Moser, Maximilian,Bristow, Helen,Jenart, Maud V. C.,Faber, Hendrik,Neophytou, Marios,Yarali, Emre,Paterson, Alexandra F.,Anthopoulos, Thomas D.,McCulloch, Iain

, p. 277 - 283 (2019/12/27)

The synthesis of a new benzocyclobutene based polymer, PSBBB, designed as a dielectric material for use in organic thin film transistors was reported. Compared to conventional benzocyclobutene-based materials, the introduction of a butoxide substituent at the 7-position of the benzocyclobutene pendant unit on the polymer allowed PSBBB to be cross-linked at temperatures of 120 °C, thus rendering it compatible with the processing requirements of flexible plastic substrates. The cross-linking behavior of PSBBB was investigated by Fourier transform infrared spectroscopy and differential scanning calorimetry, demonstrating cross-linking of the polymer after curing at 120 °C. Bottom-gate bottom-contact organic thin film transistors were fabricated using PSBBB as dielectric, affording a performance comparable to that of other dielectric polymeric materials.

An alkynylboronate cycloaddition strategy to functionalised benzyne derivatives

Kirkham, James D.,Delaney, Patrick M.,Ellames, George J.,Row, Eleanor C.,Harrity, Joseph P. A.

supporting information; experimental part, p. 5154 - 5156 (2010/10/19)

A new approach to benzyne precursors has been developed that involves the [4+2] cycloaddition of trimethylsilyl alkynylboronates with 2-pyrones, followed by oxidation and trifluoromethylsulfonylation of the boronate moiety. The Royal Society of Chemistry

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