929804-89-7 Usage
Uses
Used in Pharmaceutical Industry:
(1S)-2,2,2-Trifluoro-1-(4-fluorophenyl)ethylamine is used as a key intermediate in the synthesis of pharmaceuticals for its ability to form carbon-nitrogen bonds, which are essential in the development of new drug candidates. Its unique structural properties allow for the creation of novel compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, (1S)-2,2,2-Trifluoro-1-(4-fluorophenyl)ethylamine serves as a building block in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products. Its chemical properties make it suitable for creating compounds that can effectively target pests and enhance crop protection.
Used in Organic Synthesis:
(1S)-2,2,2-Trifluoro-1-(4-fluorophenyl)ethylamine is utilized as a reagent in organic chemistry reactions, particularly for the formation of carbon-nitrogen bonds. Its versatility in organic synthesis allows researchers to explore new pathways and create innovative compounds for various applications.
Overall, (1S)-2,2,2-Trifluoro-1-(4-fluorophenyl)ethylamine is a multifaceted compound with a broad range of potential applications across different industries, including pharmaceuticals, agrochemicals, and organic synthesis. Its unique properties and versatility make it an essential component in the development of new and improved products in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 929804-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,8,0 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 929804-89:
(8*9)+(7*2)+(6*9)+(5*8)+(4*0)+(3*4)+(2*8)+(1*9)=217
217 % 10 = 7
So 929804-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7F4N/c9-6-3-1-5(2-4-6)7(13)8(10,11)12/h1-4,7H,13H2/t7-/m0/s1
929804-89-7Relevant articles and documents
N-HETEROARYLALKYL-2-(HETEROCYCLYL AND HETEROCYCLYLMETHYL) ACETAMIDE DERIVATIVES AS SSTR4 AGONISTS
-
, (2021/10/11)
Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein L, n, R1, R2, R6, R7, R8, R9, R10, X3, X4 and X5 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, to pharmaceutical compositions which contain them, and to their use for treating diseases, disorders, and conditions associated with SSTR4.
Silver-catalyzed formal [3+2]-cycloaddition of α-trifluoromethylated methyl isocyanides: a facile stereoselective synthesis of CF3-substituted heterocycles
Zhang, Xue,Wang, Xin,Gao, Yuelei,Xu, Xianxiu
supporting information, p. 2427 - 2430 (2017/03/01)
An Ag-catalyzed formal [3+2]-cycloaddition of α-trifluoromethylated methyl isocyanides with polar double bonds has been developed for the facile access to trifluoromethylated oxazolines, imidazolines and pyrrolines under mild conditions. The practicality of this chemistry is demonstrated by the gram-scale synthesis of oxazolines with excellent yields and facile transformations of the formed oxazolines to trifluoromethylated β-amino alcohols in quantitative yields.
PYRAZOLE DERIVATIVES AS INHIBITORS OF RECEPTOR TYROSYNE KINASES
-
Page/Page column 92, (2008/06/13)
Compounds of formula (I): and their use in the inhibition of Trk activity are described.
