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344-03-6

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344-03-6 Usage

Chemical Properties

white crystalline powder

Uses

It is used as a chemical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 344-03-6 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 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 344-03:
(5*3)+(4*4)+(3*4)+(2*0)+(1*3)=46
46 % 10 = 6
So 344-03-6 is a valid CAS Registry Number.
InChI:InChI=1/C6Br2F4/c7-1-3(9)5(11)2(8)6(12)4(1)10

344-03-6 Well-known Company Product Price

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

  • (A18135)  1,4-Dibromotetrafluorobenzene, 99%   

  • 344-03-6

  • 1g

  • 375.0CNY

  • Detail
  • Alfa Aesar

  • (A18135)  1,4-Dibromotetrafluorobenzene, 99%   

  • 344-03-6

  • 5g

  • 752.0CNY

  • Detail
  • Alfa Aesar

  • (A18135)  1,4-Dibromotetrafluorobenzene, 99%   

  • 344-03-6

  • 25g

  • 2758.0CNY

  • Detail

344-03-6SDS

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 1,4-dibromo-2,3,5,6-tetrafluorobenzene

1.2 Other means of identification

Product number -
Other names Benzene,4-dibromotetrafluoro

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:344-03-6 SDS

344-03-6Relevant articles and documents

Transition-metal-free decarboxylative bromination of aromatic carboxylic acids

Quibell, Jacob M.,Perry, Gregory J. P.,Cannas, Diego M.,Larrosa, Igor

, p. 3860 - 3865 (2018/04/26)

Methods for the conversion of aliphatic acids to alkyl halides have progressed significantly over the past century, however, the analogous decarboxylative bromination of aromatic acids has remained a longstanding challenge. The development of efficient methods for the synthesis of aryl bromides is of great importance as they are versatile reagents in synthesis and are present in many functional molecules. Herein we report a transition metal-free decarboxylative bromination of aromatic acids. The reaction is applicable to many electron-rich aromatic and heteroaromatic acids which have previously proved poor substrates for Hunsdiecker-type reactions. In addition, our preliminary mechanistic study suggests that radical intermediates are not involved in this reaction, which is in contrast to classical Hunsdiecker-type reactivity. Overall, the process demonstrates a useful method for producing valuable reagents from inexpensive and abundant starting materials.

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