36556-47-5 Usage
General Description
2,3-Difluorochlorobenzene is a halogenated aromatic organic compound. As suggested by its name, its chemical structure comprises a benzene ring substituted by two fluoride atoms and one chloride atom. It is used as a reagent in various chemical reactions and synthesis processes due to its active sites that can initiate a reaction. This colorless liquid has a relatively low boiling point and moderately high melting point, making it useful in several industrial applications. Like many other organic compounds, it should be appropriately managed and handled due to its potential flammability and toxicity. It is not widely found in natural conditions and is primarily produced in laboratory settings.
Check Digit Verification of cas no
The CAS Registry Mumber 36556-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,5 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36556-47:
(7*3)+(6*6)+(5*5)+(4*5)+(3*6)+(2*4)+(1*7)=135
135 % 10 = 5
So 36556-47-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClF2/c7-4-2-1-3-5(8)6(4)9/h1-3H
36556-47-5Relevant articles and documents
Three-step regioselective synthesis of 2,3-difluorohalobenzenes using tetrafluoroethylene and buta-1,3-diene as starting building blocks
Egorov, M. P.,Lipkind, M. B.,Nefedov, O. M.,Volchkov, N. V.
, p. 925 - 932 (2021/06/07)
The gas-phase copyrolysis of tetrafluoroethylene and buta-1,3-diene in a flow tube reactor at 490–510 °C gives 3,3,4,4-tetrafluorocyclohex-1-ene, which is selectively converted to 1-bromo- or 1-chloro-2,3-difluorobenzene via intermediate steps of halogenation and dehydrohalogenation.
Method for producing tetrakis ( fluoroaryl) borate-magnesium compound
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, (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.
Preparation of substituted fluorobenzenes
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, (2008/06/13)
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