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1-(1-Bromo-2,2,2-trifluoroethyl)-4-fluorobenzene is a synthetic chemical compound characterized by its molecular formula C8H5BrF4. It is a colorless, flammable liquid that is recognized for its high reactivity and potential as a building block in the synthesis of more complex organic molecules. This halogenated aromatic hydrocarbon contains both bromine and fluorine atoms, making it a versatile intermediate in the production of pharmaceuticals and agrochemicals.

81577-15-3

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81577-15-3 Usage

Uses

Used in Pharmaceutical Industry:
1-(1-Bromo-2,2,2-trifluoroethyl)-4-fluorobenzene is used as an intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, which includes both bromine and fluorine atoms, allows for the creation of a wide range of medicinal agents with different therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(1-Bromo-2,2,2-trifluoroethyl)-4-fluorobenzene is utilized as a key intermediate in the development of new pesticides and other agricultural chemicals. Its reactivity and structural diversity contribute to the design of effective and targeted agrochemical products.
Safety Precautions:
Due to the flammability of 1-(1-Bromo-2,2,2-trifluoroethyl)-4-fluorobenzene and the potential for the release of harmful gases in the event of a fire or chemical reaction, it is crucial to handle 1-(1-Bromo-2,2,2-trifluoroethyl)-4-fluorobenzene with care. Appropriate safety measures should be taken during its production, storage, and use to minimize risks and ensure the safety of personnel and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 81577-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,7 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81577-15:
(7*8)+(6*1)+(5*5)+(4*7)+(3*7)+(2*1)+(1*5)=143
143 % 10 = 3
So 81577-15-3 is a valid CAS Registry Number.

81577-15-3Downstream Products

81577-15-3Relevant academic research and scientific papers

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

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Paragraph 0142; 0225; 0226, (2015/12/30)

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the following formula (“Formula One”).

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

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Page/Page column, (2014/06/25)

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

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Page/Page column 48; 130, (2014/07/08)

This document discloses molecules having the following formula ("Formula One"): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

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Paragraph 0648-0649, (2014/06/25)

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

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Page/Page column 71, (2013/02/28)

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

MECHANISMS OF FREE-RADICAL REACTIONS. XIII. MECHANISM AND SELECTIVITY OF THE FREE-RADICAL HALOGENATION OF ALKYL AROMATIC HYDROCARBONS WITH FLUOROALKYL SUBSTITUENTS

Dneprovskii, A. S.,Eliseenkov, E. V.,Mil'tsov, S. A.

, p. 317 - 324 (2007/10/02)

The free-radical chlorination and bromination of 1-fluoro-2-arylethanes and 1,1,1-trifluoro-2-arylethanes was studied by the method of competing reactions.In all cases a good correalation between log krel and the Brown ?+ constants was observed.The variation of the selectivity in the transition from one reaction series to the other indicates that two independent factors which determine the reactivity (the change in the dissociation energy of the C-H bond and the polar effect of the substituents) have a simultaneous effect.

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