141183-94-0 Usage
Description
4-(Perfluorooctyl)-2-methyl-2-butanol is an organic compound characterized by its perfluorinated octyl chain and a methyl butanol group. This unique molecular structure endows it with specific properties that make it suitable for various applications, particularly in the chemical synthesis and pharmaceutical industries.
Uses
Used in Chemical Synthesis:
4-(Perfluorooctyl)-2-methyl-2-butanol is used as a valuable intermediate in the highly selective two-step synthesis of (perfluoroalkyl)butanediols. Its perfluorinated chain and unique functional groups facilitate the creation of these diols, which can be further utilized in various chemical processes and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(Perfluorooctyl)-2-methyl-2-butanol may be employed as a building block for the development of novel drug candidates. Its unique structure can be leveraged to design molecules with specific biological activities, potentially leading to the discovery of new therapeutic agents.
Used in Material Science:
The perfluorinated nature of 4-(Perfluorooctyl)-2-methyl-2-butanol may also find applications in material science, where it could be used to create new materials with enhanced properties, such as improved chemical stability, thermal resistance, or reduced surface tension.
Used in Surface Treatments:
Due to its hydrophobic and oleophobic properties, 4-(Perfluorooctyl)-2-methyl-2-butanol can be used in surface treatments to create non-stick, waterand oil-repellent coatings for various applications, including industrial equipment, textiles, and consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 141183-94-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,8 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 141183-94:
(8*1)+(7*4)+(6*1)+(5*1)+(4*8)+(3*3)+(2*9)+(1*4)=110
110 % 10 = 0
So 141183-94-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H11F17O/c1-5(2,31)3-4-6(14,15)7(16,17)8(18,19)9(20,21)10(22,23)11(24,25)12(26,27)13(28,29)30/h31H,3-4H2,1-2H3
141183-94-0Relevant articles and documents
Fluorous Boc (FBoc) carbamates: New amine protecting groups for use in fluorous synthesis
Luo,Williams,Read,Curran
, p. 4261 - 4266 (2007/10/03)
The first fluorous variants of the Boc (tert-butyloxycarbonyl) group have been prepared and tested for their suitability as nitrogen protecting groups. A group with two fluorous chains and an ethylene spacer, (RfCH2CH2)2(CH3)COC(O)-, was readily attached to a representative amine but was difficult to cleave. In contrast, groups with two fluorous chains and a propylene spacer, (RfCH2CH2CH2)2-(CH3) COC(O)-, or one fluorous chain and an ethylene spacer, (RfCH2CH2)(CH3)2COC(O)-, were readily formed and cleaved. The fluorous alcohol component of the FBoc group can be removed by evaporation and can be recovered and reused. The utility of the new FBoc group (C8F17CH2CH2)(CH3) 2COC(O)- was demonstrated in 16 and 96 compound library synthesis exercises. Separations can be achieved either by manual, parallel fluorous solid-phase extraction, or automated, serial fluorous chromatography. The results provide additional confirmation of the value of "light" fluorous synthesis techniques, and the new fluorous Boc groups expand the applicability of fluorous synthesis techniques to many classes of nitrogen-containing organic compounds.
