434-39-9 Usage
Physical state
Colorless, volatile liquid
Primary use
Solvent in various chemical processes
Additional uses
Production of pharmaceuticals, agrochemicals, and other industrial chemicals
Chemical properties
Strong oxidizing properties
Application
Commonly used as a reagent in organic synthesis
Safety precautions
Handle with caution due to hazardous nature
Potential hazards
Can cause skin and eye irritation upon contact
Check Digit Verification of cas no
The CAS Registry Mumber 434-39-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 434-39:
(5*4)+(4*3)+(3*4)+(2*3)+(1*9)=59
59 % 10 = 9
So 434-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H6F3NO3/c1-2(8(10)11)3(9)4(5,6)7/h2-3,9H,1H3
434-39-9Relevant articles and documents
A convenient synthesis of trifluoromethylated pyrroles and porphyrins
Ono,Kawamura,Maruyama
, p. 3386 - 3388 (1989)
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Ψ[CH(CF3)NH]Gly-peptides: Synthesis and conformation analysis
Molteni, Marco,Bellucci, Maria Cristina,Bigotti, Serena,Mazzini, Stefania,Volonterio, Alessandro,Zanda, Matteo
scheme or table, p. 2286 - 2296 (2009/09/26)
Ψ[CH(CF3)NH]Gly peptides, a conceptually new class of peptidomimetics having a stereogenic trifluoroethylamine group as a natural peptide-bond surrogate, have been synthesized by stereoselective addition of α-amino acid esters to trans-3,3,3-tr
Solid-phase synthesis of peptidyl trifluoromethyl ketones
Poupart,Fazal,Goulet,Ly Thy Mar
, p. 1356 - 1361 (2007/10/03)
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