164411-06-7 Usage
Uses
Used in Chemical Synthesis:
Diphenylammonium trifluoromethanesulfonate is used as an efficient catalyst for the esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols. This application is particularly relevant in the chemical industry, where it aids in the greener synthesis of esters, contributing to more environmentally friendly and sustainable processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Diphenylammonium trifluoromethanesulfonate is utilized as a catalyst in the synthesis of various drugs and drug intermediates. Its high catalytic efficiency allows for faster and more selective reactions, leading to improved yields and reduced waste generation.
Used in Green Chemistry:
Diphenylammonium trifluoromethanesulfonate is used as a catalyst in green chemistry applications, where the focus is on reducing the environmental impact of chemical processes. Its ability to facilitate esterification and transesterification reactions with minimal byproducts and waste makes it a valuable component in the development of more sustainable chemical processes.
Used in Research and Development:
In research and development, Diphenylammonium trifluoromethanesulfonate is employed as a catalyst to study and optimize various chemical reactions. Its high efficiency and selectivity make it an essential tool for scientists working on the development of new compounds and materials.
Overall, Diphenylammonium trifluoromethanesulfonate is a versatile and efficient catalyst with a wide range of applications across different industries, including chemical synthesis, pharmaceuticals, green chemistry, and research and development. Its ability to facilitate esterification and transesterification reactions with high efficiency and selectivity makes it a valuable asset in the development of more sustainable and environmentally friendly chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 164411-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,4,1 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 164411-06:
(8*1)+(7*6)+(6*4)+(5*4)+(4*1)+(3*1)+(2*0)+(1*6)=107
107 % 10 = 7
So 164411-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H11N.CHF3O3S/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;2-1(3,4)8(5,6)7/h1-10,13H;(H,5,6,7)
164411-06-7Relevant academic research and scientific papers
Direct dehydrative glycosylation catalyzed by diphenylammonium triflate
Hsu, Mei-Yuan,Lam, Sarah,Lin, Mei-Huei,Lin, Su-Ching,Wang, Cheng-Chung,Wu, Chia-Hui
supporting information, (2020/03/13)
Methods for direct dehydrative glycosylations of carbohydrate hemiacetals catalyzed by diphenylammonium triflate under microwave irradiation are described. Both armed and disarmed glycosyl-C1-hemiacetal donors were efficiently glycosylated in moderate to excellent yields without the need for any drying agents and stoichiometric additives. This method has been successfully applied to a solid-phase glycosylation.
Synthesis of Complexes (1+) (L = Primary, Secondary or Tertiary Amine). Crystal Structure of *CH2Cl2
Vicente, Jose,Chicote, Maria-Teresa,Guerrero, Rita,Jones, Peter G.
, p. 1251 - 1254 (2007/10/02)
The 1:1 reaction of (Hacac = acetylacetone) with ammonium salts X (X = CF3SO3, L = 2-nitroaniline, 4-methoxyaniline, NHPh2 or NHEt2; X = ClO4, L = NMe3) in diethyl ether gave complexes X and acetylacetone.The crystal structure of was determined; orthorhombic, space group P212121, a = 9.498(2), b = 10.322(2), c = 26.154(4) Angstroem, wR(F2) 0.091.The gold atom is linearly co-ordinated to both ligands and no intermolecular Au..Au contacts exist.
97%
