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5920-84-3

Silane, [2-bromo-4,6-bis(1,1-dimethylethyl)phenoxy]trimethyl-, is a complex organic compound with the chemical formula C15H25BrOSi. It is a derivative of silane, which is a compound containing silicon and hydrogen atoms. This specific silane features a 2-bromo-4,6-bis(1,1-dimethylethyl)phenoxy group attached to a trimethylsilyl moiety. The compound is characterized by its unique structure, which includes a bromine atom, two tert-butyl groups (1,1-dimethylethyl), and a phenoxy group. This combination of functional groups gives the compound its distinct properties, making it useful in various applications, such as in the synthesis of other organic compounds or as a reagent in chemical reactions. Due to its specific structure, it is important to handle this compound with care, as it may have specific safety and storage requirements.

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  • 5920-84-3 Structure

  • Basic information

    1. Product Name: Silane, [2-bromo-4,6-bis(1,1-dimethylethyl)phenoxy]trimethyl-
    2. Synonyms:
    3. CAS NO:5920-84-3
    4. Molecular Formula: C17H29BrOSi
    5. Molecular Weight: 357.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5920-84-3.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: Silane, [2-bromo-4,6-bis(1,1-dimethylethyl)phenoxy]trimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silane, [2-bromo-4,6-bis(1,1-dimethylethyl)phenoxy]trimethyl-(5920-84-3)
    11. EPA Substance Registry System: Silane, [2-bromo-4,6-bis(1,1-dimethylethyl)phenoxy]trimethyl-(5920-84-3)

  • 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: 5920-84-3(Hazardous Substances Data)

5920-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5920-84-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5920-84:
(6*5)+(5*9)+(4*2)+(3*0)+(2*8)+(1*4)=103
103 % 10 = 3
So 5920-84-3 is a valid CAS Registry Number.

5920-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-bromo-4,6-ditert-butylphenoxy)-trimethylsilane

1.2 Other means of identification

Product number -
Other names (6-Brom-2,4-di-tert-butyl-phenoxy)-trimethyl-silan

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:5920-84-3 SDS

5920-84-3Relevant articles and documents

Microflow fluorinations of benzynes: Efficient synthesis of fluoroaromatic compounds

Ikawa, Takashi,Masuda, Shigeaki,Akai, Shuji

, p. 1153 - 1164 (2018/12/10)

Fluorinated aromatic compounds are found in a variety of biologically active compounds, including clinical drugs and agrochemicals. Therefore, the synthesis of aryl fluorides is particularly important in the medicinal and process chemistry fields. In this

Synthesis of aryl stannanes from silyl triflates via aryne intermediates

Lakshmi, B. Vasantha,Wefelscheid, Ulrike K.,Kazmaier, Uli

supporting information; experimental part, p. 345 - 348 (2011/04/15)

Aryl stannanes are easily accessible from o-silylated aryl triflates in the presence of KF and Bu3SnH. The corresponding arynes are formed in situ, and undergo clean hydrostannation to give a mixture of the regioisomeric aryl stannanes. The whole reaction sequence can also be carried out as a one-pot reaction under microwave irradiation. Georg Thieme Verlag Stuttgart New York.

Multiple intra-molecular hydrogen bonds in 2,4-di-tert-butyl-6-[N-(2,6- diisopropylphenyl)-P,P-diphenylphosphorimidoyl]phenol

Lee, Jong-Dae,Suh, Il-Hwan,Kang, Sang Ook

scheme or table, p. o151-o153 (2011/06/26)

The title compound, C38H48NOP, isolated from the reaction of (2-diphenyl-phosphanyl-4,6-di-tert-butyl)phenol with 2,6-di-iso-propyl-phenyl -azide at 273 K, can act as an N,O-bidentate ligand. Crystal structure analysis shows a deviat

Palladium(0)-catalyzed intermolecular amination of unactivated Csp 3-H bonds

Pan, Jun,Su, Mingjuan,Buchwald, Stephen L.

supporting information; experimental part, p. 8647 - 8651 (2011/11/06)

Filling out the space: The title reaction of unactivated Csp3-H bonds using aryl amines as the nitrogen source is disclosed (see scheme; dba=dibenzylideneacetone, Tf=trifluoromethanesulfonyl). Either the C-N cross-coupling product or the C-H am

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