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α,α-Difluoro-N,N-dimethylbenzylamine is an organic compound with the chemical formula C9H12F2N. It is a derivative of benzylamine, featuring two fluorine atoms attached to the alpha carbon (the carbon directly attached to the benzene ring) and two methyl groups attached to the nitrogen atom. α,α-difluoro0N,N-dimethylbenzylamine is a colorless liquid with a pungent odor and is soluble in organic solvents. It is synthesized through the reaction of benzyl chloride with dimethylamine in the presence of a fluoride source, such as potassium fluoride or sodium fluoride. α,α-Difluoro-N,N-dimethylbenzylamine has potential applications in the pharmaceutical industry as a building block for the synthesis of various drugs and agrochemicals, as well as in the production of specialty chemicals and materials. Due to its reactivity and potential toxicity, it should be handled with care and used in accordance with proper safety protocols.

702-99-8

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702-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 702-99-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 702-99:
(5*7)+(4*0)+(3*2)+(2*9)+(1*9)=68
68 % 10 = 8
So 702-99-8 is a valid CAS Registry Number.

702-99-8Relevant academic research and scientific papers

Synthesis and characterization of novel carbene complexes of phosphorus(V) fluorides with potential liquid-crystalline properties

Pajkert, Romana,B?ttcher, Tobias,Ponomarenko, Maksym,Bremer, Matthias,R?schenthaler, Gerd-Volker

, p. 8943 - 8951 (2013/09/23)

A series of novel push-push I and push-pull II carbene-stabilized complexes of phosphorus(V) fluorides bearing substituents with liquid-crystalline properties were synthesized by the oxidative addition of difluoroamines to phosphorus(III) halides. These octahedral complexes were characterized by NMR spectroscopy and X-ray analysis.

Phosphorus(V) complexes with acyclic monoaminocarbene ligands via oxidative addition

B?ttcher, Tobias,Bassil, Bassem S.,Zhechkov, Lyuben,R?schenthaler, Gerd-Volker

supporting information, p. 5651 - 5653 (2013/07/04)

(Difluoroorganyl)dimethylamines, RCF2NMe2 (R = H, Ph, tBu), can be used as carbene precursors for phosphorus trifluoride in an oxidative addition reaction. By this method, complexes of sterically nondemanding asymmetric and acyclic c

Fluorination of thiocarbon compounds with bis(2-methoxyethyl)aminosulfur trifluoride (deoxo-fluor reagent): A facile synthesis of gem-difluorides

Lal, Gauri S.,Lobach, Elyse,Evans, Ann

, p. 4830 - 4832 (2007/10/03)

A variety of thiocarbonyl derivatives (thioketone, thioester, thioamide, dithioester, and dithiocarbamate) were converted to the corresponding gem-difluorides in excellent yields on reaction with the fluorinating agent, bis(2-methoxyethyl)aminosulfur trif

REACTIONS OF N,N-DIALKYLBENZAMIDES WITH SULFUR TETRAFLUORIDE. FORMATION OF DIALKYL-α,α-DIFLUOROBENZYLAMINES

Dmowski, Wojciech,Kaminski, Maciej

, p. 1369 - 1378 (2007/10/02)

N,N-Dialkylbenzamides (1 and 3) react with sulfur tetrafluoride in presence of potassium fluoride to afford dialkyl-α,α-difluorobenzylamines (2 and 4) in good yields.The effects of the reactant structures and reaction conditions on the yield of products h

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