37178-69-1 Usage
Uses
Used in Flavoring and Fragrance Industry:
Ethyl 4-(1,1,2,2-tetrafluoroethoxy)benzoate is used as a flavoring agent in the food and beverage industry, enhancing the taste and aroma of various products. Its fruity scent also makes it a valuable ingredient in the fragrance industry, contributing to the creation of appealing scents in cosmetics and personal care products.
Used in Pharmaceutical Synthesis:
As an intermediate in the synthesis of pharmaceuticals, Ethyl 4-(1,1,2,2-tetrafluoroethoxy)benzoate plays a crucial role in the development of new drugs and organic compounds. Its unique chemical properties allow for the creation of innovative and effective medications.
Used in Chemical Synthesis:
Ethyl 4-(1,1,2,2-tetrafluoroethoxy)benzoate is also utilized as an intermediate in the synthesis of other organic compounds, showcasing its versatility in the chemical industry. Its ability to contribute to the formation of various compounds makes it a valuable asset in research and development.
Safety Precautions:
While Ethyl 4-(1,1,2,2-tetrafluoroethoxy)benzoate is stable under normal conditions, it is essential to handle it with care and store it in a cool, dry place away from sources of ignition and incompatible materials to ensure safety and maintain its stability.
Check Digit Verification of cas no
The CAS Registry Mumber 37178-69-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,7 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37178-69:
(7*3)+(6*7)+(5*1)+(4*7)+(3*8)+(2*6)+(1*9)=141
141 % 10 = 1
So 37178-69-1 is a valid CAS Registry Number.
37178-69-1Relevant academic research and scientific papers
Nucleophilic tetrafluoroethylation employing in situ formed organomagnesium reagents
Budinská, Alena,Václavík, Ji?í,Matou?ek, Václav,Beier, Petr
supporting information, p. 5844 - 5847 (2016/11/29)
Tetrafluoroalkyl bromides are metalated with equimolar iPrMgCl·LiCl (Turbo Grignard) to form organomagnesium compounds which are stable at low temperatures and react with various electrophiles (aldehydes, ketones, CO2, cyclic sulfate and sulfamidate, N-sulfonylimines, nitrone, chlorophosphate, nonaflyl azide) to afford novel functionalized tetrafluoroethylene-containing products. Ease of operation, excellent selectivity, high nucleophilicity, and enhanced stability of the reactive species together with a broad substrate scope comprise a highly attractive nucleophilic tetrafluoroethylation protocol affording unique synthetic building blocks.
Facile and efficient synthesis of fluoroalkyl aryl ethers
Kamal, Ahmed,Pratap,Ramana, K.Venkata,Ramana,Babu, A.Hari
, p. 7353 - 7355 (2007/10/03)
A convenient and practical method for the preparation of fluoroalkyl aryl ethers via substitution of iodoalkyl fluorides is described. This method involves KF complexation of the phenol, which increases the nucleophilicity of oxygen for the formation of the ether linkage.
