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1-fluoro-4-(4,4,4-trifluorobut-1-ynyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1394290-74-4

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1394290-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1394290-74-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,2,9 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1394290-74:
(9*1)+(8*3)+(7*9)+(6*4)+(5*2)+(4*9)+(3*0)+(2*7)+(1*4)=184
184 % 10 = 4
So 1394290-74-4 is a valid CAS Registry Number.

1394290-74-4Downstream Products

1394290-74-4Relevant academic research and scientific papers

To alkine and 2,2-dichloro -1, 1, 1-trifluoroethane coupling reaction for preparing the fluorine-containing of alkynes

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Paragraph 0017-0021; 0024; 0028-0029; 0043-0045, (2017/01/09)

The invention relates to a method for preparing fluorine-containing alkyne employing coupled reaction of alkyne and 2,2-dichloro-1,1,1-trifluoroethane. Particularly, cuprous alkynyl or Z-substituent alkyne, 2,2-dichloro-1,1,1-trifluoroethane and copper po

Palladium-catalyzed decarboxylative trifluoroethylation of aryl alkynyl carboxylic acids

Hwang, Jinil,Park, Kyungho,Choe, Juseok,Min, Hongkeun,Song, Kwang Ho,Lee, Sunwoo

, p. 3267 - 3271 (2014/05/06)

A trifluoroethylation of alkynes through a palladium-catalyzed decarboxylative coupling reaction was developed. When alkynyl carboxylic acids and ICH2CF3 were allowed to react with [Pd(? 3-allyl)Cl]2/XantPhos and Cs2CO3 in N,N-dimethylformamide (DMF) at 80 °C for 1 h, the desired products were formed in good yields. This catalytic system showed high functional group tolerance.

A facile parallel synthesis of trifluoroethyl-substituted alkynes

Liu, Cui-Bo,Meng, Wei,Li, Feng,Wang, Shuai,Nie, Jing,Ma, Jun-An

supporting information; experimental part, p. 6227 - 6230 (2012/08/14)

Trifluoroethylation made easy: The ease of execution of the reaction (see scheme), which runs under mild conditions and without the need for additional base or ligands, allows for the rapid parallel synthesis of a broad variety of trifluoroethylated alkynes. Both experimental and theoretical analyses indicate that the trifluoromethylcarbene could undergo concerted insertion into the Csp-H bond of the alkyne. Copyright

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