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4-bromo-6-fluorobenzene-1,3-diamine, also known as 4-bromo-6-fluoro-m-phenylenediamine, is a chemical compound with the molecular formula C6H6BrF2N2. It is a diamine derivative of benzene, featuring bromine and fluorine substituents on the 4 and 6 positions, respectively. This unique structure and properties make it a promising candidate for various applications in the fields of organic synthesis and pharmaceutical research.

166818-71-9

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166818-71-9 Usage

Uses

Used in Organic Synthesis:
4-bromo-6-fluorobenzene-1,3-diamine is used as a building block for the synthesis of various organic compounds. Its presence of bromine and fluorine atoms on the benzene ring allows for further functionalization and the creation of a wide range of chemical products.
Used in Pharmaceutical Research:
4-bromo-6-fluorobenzene-1,3-diamine is used as a starting material in the preparation of pharmaceutical intermediates. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Scientific Investigations:
Due to its potential biological activities and properties, 4-bromo-6-fluorobenzene-1,3-diamine is a subject of interest for further scientific investigations. Researchers are exploring its potential applications in various fields, including medicinal chemistry, materials science, and environmental chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 166818-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,8,1 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 166818-71:
(8*1)+(7*6)+(6*6)+(5*8)+(4*1)+(3*8)+(2*7)+(1*1)=169
169 % 10 = 9
So 166818-71-9 is a valid CAS Registry Number.

166818-71-9Downstream Products

166818-71-9Relevant academic research and scientific papers

Synthesis of 5- and 6-membered heterocycles by a strategy combining SNAr and SRN1 reactions

Beugelmans, Rene,Chbani, Mohamed

, p. 306 - 313 (2007/10/02)

The SRN1 mechanism is compatible with many substituents on the benzenic substrate and allows SRN1 reactions to be combined with SNAr reactions in a strategy which brings together their corresponding synthetic advantages.Thus, compounds containing benzene fused to 5- or 6-membered heterocycles containing N (indoles), N and P (benzazaphospholes) and N and S (benzothiazines) are readily obtained. nucleophilic aromatic substitution / SRN1 / SNAr / benzene-fused heterocycles

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