Welcome to LookChem.com Sign In|Join Free

CAS

  • or

162258-89-1

Post Buying Request

162258-89-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

162258-89-1 Usage

General Description

4-Bromo-4'-tert-butylbiphenyl is a chemical compound with the formula C16H17Br. It is a biphenyl derivative with a bromine atom attached to one of the phenyl rings and a tert-butyl group attached to the other. 4-Bromo-4'-tert-butylbiphenyl is a colorless solid that is insoluble in water but soluble in organic solvents. It is primarily used as a building block in the synthesis of other organic compounds, particularly in the field of pharmaceuticals and agrochemicals. It can also be used as a ligand in coordination chemistry and as a reagent in organic synthesis. Additionally, it has been studied for its potential as a flame retardant additive for polymers and plastics. Overall, 4-Bromo-4'-tert-butylbiphenyl has a variety of industrial and research applications due to its versatile chemical structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 162258-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,2,5 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 162258-89:
(8*1)+(7*6)+(6*2)+(5*2)+(4*5)+(3*8)+(2*8)+(1*9)=141
141 % 10 = 1
So 162258-89-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H17Br/c1-16(2,3)14-8-4-12(5-9-14)13-6-10-15(17)11-7-13/h4-11H,1-3H3

162258-89-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H27076)  4-Bromo-4'-tert-butylbiphenyl, 98%   

  • 162258-89-1

  • 1g

  • 587.0CNY

  • Detail
  • Alfa Aesar

  • (H27076)  4-Bromo-4'-tert-butylbiphenyl, 98%   

  • 162258-89-1

  • 10g

  • 3365.0CNY

  • Detail

162258-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-4'-tert-butylbiphenyl

1.2 Other means of identification

Product number -
Other names 4-Bromo-4′-tert-butylbiphenyl

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:162258-89-1 SDS

162258-89-1Relevant articles and documents

Highly Active Fe3O4@SBA-15@NHC-Pd Catalyst for Suzuki–Miyaura Cross-Coupling Reaction

?zdemir, ?smail,Akko?, Mitat,Alt?n, Serdar,Bu?day, Nesrin,Ya?ar, Sedat

, (2021/08/03)

A novel Pd-NHC functionalized magnetic Fe3O4@SBA-15@NHC-Pd was synthesized and used as an efficient heterogeneous catalyst in the Suzuki–Miyaura C–C bond formation reactions. The Fe3O4@SBA-15@NHC-Pd characterized by X-Ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Fourier Transform Infrared (FTIR) spectroscopy, Scanning Electron Microscopy (SEM), Transmission Electron Microscopy?(TEM), Energy Dispersive X-ray analysis (EDX), Thermogravimetric Analysis (TGA), Differential Thermal Analysis (DTA). The Inductively Coupled Plasma-Optical emission spectroscopy (ICP-OES)?analysis was used to determine the exact amount of Pd (0.33?wt%) in Fe3O4@SBA-15@NHC-Pd. The TEM images of the catalyst showed the existence of palladium nanoparticles immobilized in the catalyst's structure, while no reducing agent was used. The NHC moieties in the catalyst structure could be stabilize Pd(0) nanoparticles prevents agglomeration. The magnetic catalyst was effectively used in the Suzuki–Miyaura cross-coupling reaction of substituted phenylboronic acid derivatives with (hetero)aryl bromides in the presence of a K2CO3 at room temperature in aqueous media and magnetic catalyst could be simply extracted from the reaction mixture by an external magnet. Different aryl bromides were converted to coupled-products in excellent yields with spectacular TOFs values (up to 1,960,339?h?1); in the presence of 1?mg of Fe3O4@SBA-15@NHC-Pd catalyst (contains 3.1 × 10–6?mol% Pd) at room temperature in aqueous media. After reusability experiments, it is found that this catalyst was effectively used up to ten times in the reaction with almost consistent catalytic efficiency. A decrease in the activity of the 10th reused catalyst was found as 9%. Graphic Abstract: [Figure not available: see fulltext.]

Arylation of aryllithiums with: S-arylphenothiazinium ions for biaryl synthesis

Morofuji, Tatsuya,Yoshida, Tatsuki,Tsutsumi, Ryosuke,Yamanaka, Masahiro,Kano, Naokazu

supporting information, p. 13995 - 13998 (2020/11/21)

Aryllithiums are one of the most common and important aryl nucleophiles; nevertheless, methods for arylation of aryllithums to produce biaryls have been limited. Herein, we report arylation of aryllithiums with S-arylphenothiazinium ions through selective

Novel compound and organic light emitting device comprising the same

-

Paragraph 0161; 0162-0164, (2020/09/12)

The present invention provides a novel compound and an organic light emitting device using the same, wherein the compound is represented by chemical formula 1. The compound may improve life characteristics of the organic light emitting device.COPYRIGHT KIPO 2021

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 162258-89-1