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(3-bromo-2-fluorophenyl)(methyl)sulfane is a chemical compound that features a fluorine and bromine-substituted phenyl ring connected to a methylsulfane group. This unique structure, with its combination of fluorine, bromine, and sulfur atoms, positions it as a valuable building block for the synthesis of new compounds with a range of properties and applications.

871353-01-4

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871353-01-4 Usage

Uses

Used in Organic Synthesis:
(3-bromo-2-fluorophenyl)(methyl)sulfane is utilized as a reagent in organic synthesis for the introduction of sulfur-containing functional groups into organic molecules. Its presence allows for the creation of a variety of sulfur-containing compounds, which can be crucial for the development of new materials and pharmaceuticals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (3-bromo-2-fluorophenyl)(methyl)sulfane is used as a key intermediate in the synthesis of drugs. Its unique structure can contribute to the development of new therapeutic agents with improved pharmacological properties, such as enhanced bioavailability, selectivity, and potency.
Used in Agrochemicals:
(3-bromo-2-fluorophenyl)(methyl)sulfane also finds application in the agrochemical sector, where it can be used as a precursor for the development of new pesticides or other agricultural chemicals. Its ability to introduce sulfur-containing groups can lead to the creation of more effective and environmentally friendly products.
Used in Materials Science:
In the field of materials science, (3-bromo-2-fluorophenyl)(methyl)sulfane is employed in the development of novel materials with specific properties. The incorporation of sulfur can lead to materials with improved mechanical, thermal, or electrical characteristics, depending on the application.
Further research is necessary to fully explore the potential uses and effects of (3-bromo-2-fluorophenyl)(methyl)sulfane, as its unique combination of elements can lead to the discovery of new applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 871353-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,3,5 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 871353-01:
(8*8)+(7*7)+(6*1)+(5*3)+(4*5)+(3*3)+(2*0)+(1*1)=164
164 % 10 = 4
So 871353-01-4 is a valid CAS Registry Number.

871353-01-4Relevant academic research and scientific papers

Sodiation of Arenes and Heteroarenes in Continuous Flow

Weidmann, Niels,Ketels, Marthe,Knochel, Paul

supporting information, p. 10748 - 10751 (2018/07/30)

The first sodiations of (hetero)arenes in continuous flow using NaDA (sodium diisopropylamide) in Me2EtN are reported. This flow procedure enables sodiation of functionalized arenes and heteroarenes that decompose under batch-sodiation conditions. The resulting sodiated (hetero)arenes react instantly with various electrophiles, such as ketones, aldehydes, isocyanates, alkyl bromides, and disulfides, affording polyfunctionalized (hetero)arenes in high yields. Scale-up is possible without further optimization.

INDAZOLYL-PYRIMIDINES AS KINASE INHIBITORS

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Page/Page column 48-49, (2011/10/13)

Disclosed are compounds having the formula: or a salt thereof, wherein A, n, R1, R1A, and R2 are as defined herein, and methods of making and using the same.

PROCESS FOR THE SYNTHESIS OF 4-(3-SULFONYLPHENYL)-PIPERIDINES

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Page/Page column 15-16, (2010/11/08)

The present invention is directed to processes for the preparation of 4-(sulfonylphenyl)-piperidines of the Formula (VI), and pharmaceutically acceptable salts thereof; which comprises oxidizing a sulfide of the Formula (VII) or Formula (VIII), to give a

NEW DISUBSTITUTED PHENYLPIPERIDINES/PIPERAZINES AS MODULATORS OF DOPAMINE NEUROTRANSMISSION

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Page/Page column 58-59, (2008/06/13)

The present invention relates to compounds which have therapeutic effects against disorders in the central nervous system, and in particular new 4-(ortho, meta-disubstituted phenyl)-1-alkypiperidines and piperazines. (I) wherein R1, R2, R3 and Y are as de

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