70253-78-0 Usage
General Description
2,2,2-Trifluoroethyl laurate is a chemical compound with the molecular formula C14H25F3O2. It is a clear, colorless liquid that is insoluble in water but soluble in organic solvents. 2,2,2-TRIFLUOROETHYL LAURATE is commonly used as a surfactant or emulsifier in various industrial applications, particularly in the production of cosmetics, personal care products, and pharmaceuticals. It is also utilized in the manufacturing of polymers and as a processing aid in the production of polymers and plastics. Additionally, 2,2,2-Trifluoroethyl laurate has potential applications in the agricultural sector as a pesticide or herbicide formulation ingredient. However, due to its chemical properties and potential risks to human health and the environment, proper handling and disposal procedures are necessary when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 70253-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,5 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70253-78:
(7*7)+(6*0)+(5*2)+(4*5)+(3*3)+(2*7)+(1*8)=110
110 % 10 = 0
So 70253-78-0 is a valid CAS Registry Number.
70253-78-0Relevant articles and documents
Method for preparing fatty acid trifluoro-ethyl ester without catalysts or condensation agents
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Paragraph 0024; 0025, (2017/07/01)
The invention discloses a method for preparing fatty acid trifluoro-ethyl ester without catalysts or condensation agents. The method includes steps of mixing fatty acid and alkali with each other to obtain mixtures; adding trifluoro-ethyl aryl trivalence iodine reagents into the mixtures; carrying out stirring reaction at the temperatures ranging from -20 DEC C to 100 DEG C for 1-72 h to obtain reaction products. A molar ratio of the fatty acid to the trifluoro-ethyl aryl trivalence iodine reagents is 1:(0.2-5); a molar ratio of the fatty acid to the alkali is 1:(0.2-5). The method has the advantages that the catalysts and the condensation agents can be omitted, and even organic solvents can be omitted; the trifluoro-ethylation reagents PhICH2CF3[X] can be conveniently synthesized from CF3H2I; raw materials for the fatty acid trifluoro-ethyl ester are easily available, reaction conditions are mild, functional groups are good in compatibility, substrates are wide in application range, the method is easy to implement, and the target products nearly can be obtained under the condition of quantitative yields.
