2968-33-4 Usage
Uses
Used in Pharmaceutical Industry:
3,3,3-Trifluoropropylamine hydrochloride is used as a reagent for the production of pharmaceuticals, given its role in the synthesis of a wide range of medicinal compounds. Its incorporation into drug molecules can enhance their properties, such as solubility and bioavailability, making it an essential component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 3,3,3-Trifluoropropylamine hydrochloride is utilized as a reagent in the synthesis of agrochemicals. Its contribution to the development of effective and targeted pesticides and herbicides is significant, as it can improve the performance and selectivity of these products.
Used in Specialty Chemicals Industry:
3,3,3-Trifluoropropylamine hydrochloride is used as a building block in the synthesis of specialty chemicals, including surfactants and other complex organic compounds. Its presence in these molecules can impart unique properties, such as increased stability and reactivity, which are valuable in various industrial applications.
Used in Organic Compounds Synthesis:
As a versatile chemical intermediate, 3,3,3-Trifluoropropylamine hydrochloride is used in the synthesis of various organic compounds, particularly fluorinated ones. These compounds are valuable in the pharmaceutical and agrochemical industries due to their unique chemical and biological properties, which can be harnessed for the development of innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 2968-33-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2968-33:
(6*2)+(5*9)+(4*6)+(3*8)+(2*3)+(1*3)=114
114 % 10 = 4
So 2968-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H6F3N.ClH/c4-3(5,6)1-2-7;/h1-2,7H2;1H
2968-33-4Relevant academic research and scientific papers
Josse, Olivier,Labar, Daniel,Georges, Benoit,Grégoire, Vincent,Marchand-Brynaert, Jacqueline
, p. 665 - 675 (2001)
[18F]-2-(2-Nitroimidazol-1-yl)-N-(3,3,3-trifluoropropyl)-acetamide ([18F]-EF3) has been prepared, in 65% chemical yield and 5% radiochemical yield, by coupling 2,3,5,6-tetrafluorophenyl 2-(2-nitroimidazol-1-yl) acetate 1 with [18F]-3,3,3-trifluoropropylamine 7. This original radiolabelled key-synthon was obtained in 40% overall chemical yield by oxidative [18F]-fluorodesulfurization of ethyl N-phthalimido-3-aminopropane dithioate 4, followed by deprotection with hydrazine of the resulting [18F]-N-phthalimido-3,3,3-trifluoropropylamine 5. All the process was performed within 90min, from the [18F]-HF production in the cyclotron to the purification of the final target. Copyright
