141483-15-0 Usage
Description
2-Fluoro-5-(trifluoromethyl)phenol is an organic fluorinated building block, characterized by its clear colorless to orange liquid appearance. It is a compound that holds potential in various applications due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
2-Fluoro-5-(trifluoromethyl)phenol is used as an intermediate for the synthesis of various pharmaceutical compounds. Its fluorinated structure contributes to the development of new drugs with improved pharmacological properties, such as enhanced bioavailability and selectivity.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-Fluoro-5-(trifluoromethyl)phenol serves as a key building block for creating a range of fluorinated organic compounds. These compounds find applications in various industries, including agrochemicals, materials science, and specialty chemicals.
Used in Material Science:
2-Fluoro-5-(trifluoromethyl)phenol is used as a component in the development of advanced materials with specific properties, such as high thermal stability, chemical resistance, and low surface energy. These materials can be utilized in coatings, adhesives, and other industrial applications.
Used in Agrochemicals:
In the agrochemical industry, 2-Fluoro-5-(trifluoromethyl)phenol is used as a starting material for the synthesis of novel pesticides and herbicides. Its fluorinated nature can lead to the creation of more effective and environmentally friendly agrochemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 141483-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,4,8 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141483-15:
(8*1)+(7*4)+(6*1)+(5*4)+(4*8)+(3*3)+(2*1)+(1*5)=110
110 % 10 = 0
So 141483-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H4F4O/c8-5-2-1-4(3-6(5)12)7(9,10)11/h1-3,12H
141483-15-0Relevant articles and documents
Pd-Catalyzed debenzylation and deallylation of ethers and esters with sodium hydride
Mao, Yujian,Liu, Ye,Hu, Yanwei,Wang, Liang,Zhang, Shilei,Wang, Wei
, p. 3016 - 3020 (2018/04/14)
Herein we demonstrate simply that the addition of Pd(OAc)2 as a promotor switches the reactivity of a commonly used base NaH to a nucleophilic reductant. The reactivity is engineered into a palladium-catalyzed reductive debenzylation and deallylation of aryl ethers and esters. This operationally simple, mild protocol displays a broad substrate scope and a broad spectrum of functional group tolerance (>50 examples) and high chemoselectivity toward aryl ethers over aliphatic structures. Moreover, the dual reactivity of NaH as a base and a reductant is demonstrated in efficient synthetic elaboration.
6-(Nonsubstituted or substituted) phenoxy picolinic acids, process of preparing the same, and agricultural/horticultural germicides containing the same
-
, (2008/06/13)
An agricultural or horticultural fungicide containing 6-(unsubstituted or substituted) phenoxy picolinic acid represented by the general formula (I), as an effective ingredient. wherein R is a halogen atom, a C1to C4alkyl group, a C1to C4haloalkyl group, a C1to C4alkoxy group, a C1to C4haloalkoxy group, a C1to C4alkylthio group, a C1to C4alkylamino group, a di(C1to C4alkyl)amino group or a C7to C8aralkyl(C1to C4alkyl)amino group; n2is an integer of 0 to 3; Y is a C1to C4alkyl group, a C1to C4haloalkyl group, a C1to C4alkoxy group, a C1to C4haloalkoxy group, a C1to C4alkylthio group, a C1to C4haloalkylthio group or a halogen atom; and m is an integer of 0 to 5, and when m and n2are not less than 2, Rs and Ys may be the same or different, respectively. The compound is useful as an effective ingredient of agricultural or horticultural fungicides.
