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Benzen-2,6-d2-amine, 4-fluoro, also known as 4-fluoro-2,6-d2-aniline or 4-fluoro-2,6-D2-phenylamine, is a chemical compound with the molecular formula C6D2H4FN. It is a deuterated derivative of 4-fluoroaniline, where two hydrogen atoms are replaced by deuterium atoms. Benzen-2,6-d2-amine, 4-fluoro- is primarily used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The presence of the fluorine atom and deuterium atoms in the molecule can influence its reactivity, stability, and other properties, making it a valuable intermediate in organic synthesis.

2557-69-9

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2557-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2557-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2557-69:
(6*2)+(5*5)+(4*5)+(3*7)+(2*6)+(1*9)=99
99 % 10 = 9
So 2557-69-9 is a valid CAS Registry Number.

2557-69-9Relevant academic research and scientific papers

A substituted boron-containing compounds and pharmaceutical compositions containing the compounds (by machine translation)

-

Paragraph 0168; 0170; 0171; 0172; 0173, (2019/02/02)

The present invention provides a substituted boron-containing compounds and containing the compound of the pharmaceutical composition and its use, the boron-containing compound of the formula (I) compounds, or their pharmaceutically acceptable salt, prodr

Gold-catalyzed oxidative coupling of arylsilanes and arenes: Origin of selectivity and improved precatalyst

Ball, Liam T.,Lloyd-Jones, Guy C.,Russell, Christopher A.

supporting information, p. 254 - 264 (2014/01/23)

The mechanism of gold-catalyzed coupling of arenes with aryltrimethylsilanes has been investigated, employing an improved precatalyst (thtAuBr3) to facilitate kinetic analysis. In combination with linear free-energy relationships, kinetic isotope effects, and stoichiometric experiments, the data support a mechanism involving an Au(I)/Au(III) redox cycle in which sequential electrophilic aromatic substitution of the arylsilane and the arene by Au(III) precedes product-forming reductive elimination and subsequent cycle-closing reoxidation of the metal. Despite the fundamental mechanistic similarities between the two auration events, high selectivity is observed for heterocoupling (C-Si then C-H auration) over homocoupling of either the arylsilane or the arene (C-Si then C-Si, or C-H then C-H auration); this chemoselectivity originates from differences in the product-determining elementary steps of each electrophilic substitution. The turnover-limiting step of the reaction involves associative substitution en route to an arene π-complex. The ramifications of this insight for implementation of the methodology are discussed.

STUDY OF THE ORIENTATIONAL ORDER AND DYNAMICS IN THE NEMATIC AND SMECTIC PHASES OF p'-HEXYLOXYBENZYLIDEN-p-FLUOROANILINE BY MEANS OF 2H-NMR

Forte, Claudia,Gandolfo, Concetta,Geppi, Marco,Veracini, Carlo Alberto

, p. 213 - 228 (2007/10/03)

Measurements of orientational order parameters and spectral densities of motion in the nematic, smectic A and smectic B phases of p'-hexyloxybenzyliden-p-fluoroaniline, fully deuterated in the chain and partially deuterated in the aniline ring, are report

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