Welcome to LookChem.com Sign In|Join Free

CAS

  • or

348-61-8

Post Buying Request

348-61-8 Suppliers

Recommended suppliersmore

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

348-61-8 Usage

Chemical Properties

clear colorless to pale yellow liquid

Uses

Different sources of media describe the Uses of 348-61-8 differently. You can refer to the following data:
1. Intermediates of Liquid Crystals
2. 4-Bromo-1,2-difluorobenzene has been used in the preparation of 4-benzyl-2-(3,4-difluorophenyl)-2-hydroxy-morpholine.

General Description

Regioselective nucleophilic aromatic substitution reaction of 4-bromo-1,2-difluorobenzene with benzyl alcohol has been investigated.

Check Digit Verification of cas no

The CAS Registry Mumber 348-61-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 348-61:
(5*3)+(4*4)+(3*8)+(2*6)+(1*1)=68
68 % 10 = 8
So 348-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H3BrF2/c7-4-1-2-5(8)6(9)3-4/h1-3H

348-61-8 Well-known Company Product Price

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

  • (A11934)  4-Bromo-1,2-difluorobenzene, 98+%   

  • 348-61-8

  • 5g

  • 297.0CNY

  • Detail
  • Alfa Aesar

  • (A11934)  4-Bromo-1,2-difluorobenzene, 98+%   

  • 348-61-8

  • 25g

  • 1363.0CNY

  • Detail
  • Alfa Aesar

  • (A11934)  4-Bromo-1,2-difluorobenzene, 98+%   

  • 348-61-8

  • 100g

  • 2604.0CNY

  • Detail

348-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Bromo-3,4-difluorobenzene

1.2 Other means of identification

Product number -
Other names 1-BroMo-3

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:348-61-8 SDS

348-61-8Relevant articles and documents

High-throughput Synthesis and Screening of Iridium(III) Photocatalysts for the Fast and Chemoselective Dehalogenation of Aryl Bromides

Bernhard, Stefan,Connell, Timothy U.,Diluzio, Stephen,Kowalewski, Jakub F.,Kowalewski, Tomasz,Lewis, Jacqueline,Mdluli, Velabo,Yaron, David

, p. 6977 - 6987 (2020)

A high-throughput optical screening method for the photocatalytic activity of a structurally diverse library of 1152 cationic iridium(III) complexes ([Ir(C^N)2(N^N)]+), corresponding to all combinations of 48 cyclometalating (C^N) and 24 ancillary (N^N) ligands, was developed. This rapid assay utilizes the colorimetric changes of a high contrast indicator dye, coumarin 6, to monitor the photo-induced electron transfer from a sacrificial amine donor to the metal complex excited state. The resulting [Ir(C^N)2(N^N)]0 can then reduce an aryl bromide to form the highly reactive aryl radical intermediate. The rate of this reaction is dictated by the molecular structure of both coordinating ligands. Relative reaction rate constants determined via this method correlated closely with 19F NMR measurements obtained using a fluorinated substrate. A simple model that expresses the rate constant as a product of a single ″strength″ parameter assigned to each of the 72 ligands can well account for the 1152 measured rate constants. The best performing complexes exhibit much higher reactivity than the benchmark photocatalysts commonly used in photoredox transformations. The catalysts were also successfully tested for their chemoselectivity. The developed screening methodology can enable generation of the large data sets needed to use modern data science to extract structure-activity relationships.

PROCESS FOR THE PREPARATION OF ORGANIC BROMIDES

-

Paragraph 00139, (2017/07/28)

The present invention provides a process for the preparation of organic bromides, by a radical bromodecarboxylation of carboxylic acids with a bromoisocyanurate.

Bromination of aromatic compounds using an Fe2O 3/zeolite catalyst

Nishina, Yuta,Takami, Keishi

supporting information, p. 2380 - 2383 (2013/02/21)

The catalytic bromination of non-activated aromatic compounds has been achieved using an Fe2O3/zeolite catalyst system. FeBr 3 was identified as the catalytic species, formed in situ from HBr and Fe2O3. The catalyst was easy-to-handle and cost effective and could also be recycled. The reaction system was also amenable to the one-pot sequential bromination/C-C bond formation of benzene.

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 348-61-8