2367-76-2 Usage
Description
1-Bromo-2,4,6-trifluorobenzene is an organic compound that exhibits packing polymorphism in two nonidentical solid-state phases. It is a clear colorless liquid and is known to participate in Pd-catalyzed oxidative Heck reactions with allyl ester.
Uses
Used in Pharmaceutical Industry:
1-Bromo-2,4,6-trifluorobenzene is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block in the development of new drugs.
Used in Chemical Synthesis:
1-Bromo-2,4,6-trifluorobenzene is used as a reactant in the Pd-catalyzed oxidative Heck reaction with allyl ester. This reaction is an important method for the formation of carbon-carbon bonds, which are crucial in the synthesis of complex organic molecules.
Used in Material Science:
Due to its packing polymorphism, 1-Bromo-2,4,6-trifluorobenzene can be utilized in the development of novel materials with unique properties. The ability to exist in different solid-state phases allows for the exploration of its potential applications in areas such as crystal engineering and material design.
Used in Research and Development:
1-Bromo-2,4,6-trifluorobenzene serves as a valuable compound for research purposes, particularly in the fields of organic chemistry, medicinal chemistry, and materials science. Its unique properties and reactivity make it an interesting subject for further study and potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2367-76-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2367-76:
(6*2)+(5*3)+(4*6)+(3*7)+(2*7)+(1*6)=92
92 % 10 = 2
So 2367-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl2F2/c7-4-1-3(9)2-5(8)6(4)10/h1-2H
2367-76-2Relevant articles and documents
PROCESS FOR PREPARATION OF HALO SUBSTITUTED BENZOIC ACID COMPOUND AND INTERMEDIATES THEREOF
-
Page/Page column 13, (2018/09/28)
The present invention provides a process for preparation of halo substituted benzoic acid compound of Formula (1) and intermediates thereof.
Method for the production of substituted 2-aryl malonic acid esters
-
Page/Page column 4, (2010/04/23)
The present invention relates to a process for preparing substituted 2-arylmalonic esters of the general formula I in which R is C1-C6-alkyl or C1-C4-alkoxy-C1-C4-alkyl; Ar is phenyl or a heteroaromatic 5- or 6-membered ring; where each carbon atom present in the radicals mentioned above optionally carries a substituent RA; RA is F, Cl, CN, NO2, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, etc., or two adjacent substituents RA together with the carbon atoms to which they are attached form a ring; and where a malonic ester is reacted with a base and an aryl bromide in the presence of a copper salt, which comprises employing from 0.1 to 0.65 molar equivalents of the base per molar equivalent of the malonic ester.
Method for producing tetrakis ( fluoroaryl) borate-magnesium compound
-
, (2008/06/13)
Fluoroaryl magnesium halide is reacted with a boron compound so that a molar ratio of the fluoroaryl magnesium halide to the boron compound is not less than 3.0 and not more than 3.7, so as to produce a tetrakis (fluoroaryl) borate·magnesium compound. With this method, there occurs no hydrogen fluoride which corrodes a producing apparatus and requires troublesome waste water treatment.