1428-54-2 Usage
Description
2-[3-(trifluoromethyl)phenyl]oxirane, also known as 3-(Trifluoromethyl)phenyl glycidyl ether, is a chemical compound with the molecular formula C9H7F3O. It is a colorless, clear liquid with a sweet odor and is soluble in organic solvents. 2-[3-(trifluoromethyl)phenyl]oxirane is often used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals.
Uses
Used in Pharmaceutical Industry:
2-[3-(trifluoromethyl)phenyl]oxirane is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 2-[3-(trifluoromethyl)phenyl]oxirane is used as an intermediate in the production of pesticides and other agrochemicals, helping to create effective compounds for crop protection and enhancement of agricultural yields.
Used in Specialty Chemicals Industry:
2-[3-(trifluoromethyl)phenyl]oxirane is utilized as an intermediate in the synthesis of specialty chemicals, which are high-value compounds used in various applications such as coatings, adhesives, and advanced materials.
It is important to handle 2-[3-(trifluoromethyl)phenyl]oxirane with care, as it can be harmful if swallowed, inhaled, or in contact with skin and eyes. Additionally, it may cause respiratory irritation and central nervous system depression if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 1428-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1428-54:
(6*1)+(5*4)+(4*2)+(3*8)+(2*5)+(1*4)=72
72 % 10 = 2
So 1428-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3O/c10-9(11,12)7-3-1-2-6(4-7)8-5-13-8/h1-4,8H,5H2
1428-54-2Relevant articles and documents
Regio- and chemoselective rearrangement of terminal epoxides into methyl alkyl and aryl ketones
Tian, Yingying,Jürgens, Eva,Kunz, Doris
supporting information, p. 11340 - 11343 (2018/10/31)
The development of the highly active pincer-type rhodium catalyst 2 for the nucleophilic Meinwald rearrangement of functionalised terminal epoxides into methyl ketones under mild conditions is presented. An excellent regio- and chemoselectivity is obtained for the first time for aryl oxiranes.
Molecular ruthenium complexes anchored on magnetic nanoparticles that act as powerful and magnetically recyclable stereospecific epoxidation catalysts
Vaquer, Lydia,Riente, Paola,Sala, Xavier,Jansat, Susanna,Benet-Buchholz, Jordi,Llobet, Antoni,Pericas, Miquel A.
, p. 706 - 714 (2013/03/29)
Two new Ru-aqua complexes containing a phosphonated trpy ligand with the general formula [Ru(trpy-P)(B)(H2O)]2+ (trpy-P is diethyl [2,2′:6′,2″-terpyridin]-4′-ylphosphonate (1); B = bpm (5a) is 2,2′-bipyrimidine; (or) B = azpy (cis- a