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2-Fluoro-2-methylbutane, also known as tert-butyl fluoride or 2,2-difluoropentane, is a colorless, volatile liquid with the chemical formula C5H11F. It is an organic compound that belongs to the alkane family, specifically a branched-chain alkane with a fluorine atom replacing one of the hydrogen atoms. This fluorinated alkane is used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential health and environmental concerns, it is typically handled with care in controlled laboratory settings.

661-53-0

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661-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 661-53-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 661-53:
(5*6)+(4*6)+(3*1)+(2*5)+(1*3)=70
70 % 10 = 0
So 661-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H11F/c1-4-5(2,3)6/h4H2,1-3H3

661-53-0Downstream Products

661-53-0Relevant academic research and scientific papers

Determination and interpretation of second order rate constants for the addition of hydrogen halides to alkenes

Borgeaud, Robert,Newman, Henry,Schelpe, Arabella,Vasco, Veronica,Peter Hughes

, p. 810 - 813 (2007/10/03)

An extensive range of second order rate constants for the addition of hydrogen halides to alkenes in 98% v/v ethanoic acid (acetic acid)-water have been obtained by conductivity measurements. The rate constants are in the expected order of HF HCl HBr HI. The rates with different alkenes cannot be rationalised solely by a consideration of carbocation stability and it has been necessary to consider steric effects in order to explain the observed order.

THE REACTION OF PERFLUOROBUTANESULFONYL FLUORIDE WITH ALCOHOLS IN THE PRESENCE OF 4-DIALKYLAMINOPYRIDINES

Bennua-Skalmowski, Baerbel,Krolikiewicz, Konrad,Vorbrueggen, Helmut

, p. 453 - 462 (2007/10/02)

Primary hydroxy groups as in neopentyl alcohol 7 or neopentylglycol 18 react readily with perfluorobutanesulfonyl fluoride 1 in the presence of 2 equiv. of the nucleophilic 4-dialkylaminopyridines 4 to afford high yields of the corresponding N-alkyl-4-dialkylaminopyridinium perfluorobutanesulfonates (nonaflates).Secondary hydroxy groups give rise to a mixture of the corresponding olefins and monofluorides as well as of the corresponding N-alkyl-4-dialkylaminopyridinium nonaflates.

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