91944-47-7 Usage
Uses
Used in Pharmaceutical Industry:
Trifluoropyruvic aldehyde is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure and reactivity allow for the creation of novel compounds with potential medicinal applications.
Used in Agrochemical Industry:
In the agrochemical sector, trifluoropyruvic aldehyde is employed as an intermediate for the production of pesticides and other agrochemicals. Its involvement in the synthesis of these compounds helps in the development of effective solutions for agricultural challenges.
Used in Organic Synthesis:
Trifluoropyruvic aldehyde is utilized as a key component in organic synthesis, where its high reactivity enables the formation of a diverse array of chemical products. This makes it a valuable asset in the creation of new compounds for various applications.
Used as a Reagent in Fluorinated Compounds Synthesis:
As a reagent, trifluoropyruvic aldehyde is instrumental in the synthesis of fluorinated compounds. Its role in this process is crucial for the development of new materials with unique properties, which can be applied across different industries.
Used in Medicinal Chemistry Research:
Due to its distinctive structure and properties, trifluoropyruvic aldehyde has potential applications in the field of medicinal chemistry. It is used in research to explore its capabilities in the development of new pharmaceutical agents and to enhance our understanding of its interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 91944-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,4 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91944-47:
(7*9)+(6*1)+(5*9)+(4*4)+(3*4)+(2*4)+(1*7)=157
157 % 10 = 7
So 91944-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C3HF3O2/c4-3(5,6)2(8)1-7/h1H
91944-47-7Relevant academic research and scientific papers
Carr, Sinead,Shallcross, Dudley E.,Canosa-Mas, Carlos E.,Wenger, John C.,Sidebottom, Howard W.,Treacy, Jack J.,Wayne, Richard P.
, p. 3874 - 3883 (2003)
Rate coefficients for the reactions of hydroxyl radicals and chlorine atoms with a series of halogenated acetones of the type CX3COCH 3 (X = H, Cl, F) have been determined using a photolytic relative-rate technique at T = 298 K and at 760 Torr total pressure. The reactions studied and the rate coefficients obtained are shown in the table. Reaction Reaction number Rate coefficient/cm3 molecule-1 s-1 OH + CH3COCH3 → products (1) (2.2 ± 0.5) × 10-13 OH + CH2ClCOCH3 → products (2) (4.2 ± 0.8) × 10-13 OH + CHCl 2COCH3 → products (3) (3.8 ± 0.8) × 10-13 OH + CCl3COCH3 → products (4) (1.5 ± 0.3) × 10-14 OH + CH2FCOCH3 → products (5) (2.1 ± 0.4) × 10-13 OH + CF 3COCH3 → products (6) (6.9 ± 1.3) × 10-15 Cl + CH3COCH3 → products (7) (2.2 ± 0.4) × 10-12 Cl + CH2ClCOCH3 → products (8) (2.0 ± 0.2) × 10-12 Cl + CHCl 2COCH3 → products (9) (1.7 ± 0.3) × 10-13 Cl + CCl3COCH3 → products (10) ( 1. 7 ± 0.3) × 10-14 Cl + CH2FCOCH3 → products (11) (8.2 ± 1.6) × 10-13 Cl + CF 3COCH3 → products (12) (8.0 ± 1.6) × 10-15 The errors quoted reflect an estimate of the absolute uncertainty in the measured rate coefficients of ±20%. For reactions (7)-(12), Fourier transform infrared spectroscopy was used to identify products. Qualitative ultra-violet absorption spectra were also recorded for most of the halogenated species investigated in this study, and have been used together with the kinetic data to derive atmospheric lifetimes for these species.
