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1-(difluoromethyl)-4-(dimethylamino)benzol, also known as 4-(dimethylamino)benzene-1-difluoromethyl, is an organic compound with the molecular formula C9H10F2N. It is a derivative of benzene, featuring a difluoromethyl group (-CF2H) at the 1-position and a dimethylamino group (-N(CH3)2) at the 4-position. This chemical is characterized by its fluorinated and amino substituents, which can influence its reactivity, solubility, and other physical properties. It may be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structural features.

705-39-5

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705-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 705-39-5 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 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 705-39:
(5*7)+(4*0)+(3*5)+(2*3)+(1*9)=65
65 % 10 = 5
So 705-39-5 is a valid CAS Registry Number.

705-39-5Downstream Products

705-39-5Relevant academic research and scientific papers

Sandmeyer difluoromethylation of (hetero-)arenediazonium salts

Matheis, Christian,Jouvin, Kvin,Goossen, Lukas J.

, p. 5984 - 5987 (2014)

A Sandmeyer-type difluoromethylation process has been developed that allows the straightforward conversion of (hetero-)arenediazonium salts into the corresponding difluoromethyl (hetero-)arenes under mild conditions. The actual difluoromethylating reagent, a difluoromethyl-copper complex, is formed in situ from copper thiocyanate and TMS-CF2H. The diazonium salts are either preformed or generated in situ from broadly available aromatic amines.

METHOD AND REAGENT FOR DEOXYFLUORINATION

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Paragraph 0148-0150; 0152-0153, (2021/05/29)

A safe, simple, and selective method and reagent for deoxyfluorination is disclosed. With the method and reagent disclosed herein, organic compounds such as carboxylic acids, carboxylates, carboxylic acid anhydrides, aldehydes, and alcohols can be fluorinated by using the most common nucleophilic fluorinating reagents and electron deficient fluoroarenes as mediators under mild conditions, giving corresponding fluoroorganic compounds in excellent yield with a wide range of functional group compatibility and easy product purification. For example, directly utilizing KF for deoxyfluorination of carboxylic acids provides the most economical and the safest pathway to access acyl fluorides, key intermediates for syntheses of peptide, amide, ester, and dry fluoride salts.

Syntheses of New Aromatic Compounds with Fluorinated Side Chains and their Chemical Reactivity

Haas, Alois,Spitzer, Martin,Lieb, Max

, p. 1329 - 1340 (2007/10/02)

The syntheses of a wide range of aromatic compounds of the type p-Y-C6H4CF2X(4-13) are described, and the chemical behavior of these compounds as a function of substituent Y is investigated .Analogously the pyridine derivatives 15, 17, and 18 were synthesized and characterized.From a correlation of the 19F-NMR data of these compounds with the Hammett constant of Y, participation of C-F ?-back-donation is seen as the cause for an observed shift of the 19F signals to lower field.

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