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The chemical compound "2,2,3,3,3-Pentafluoro-propionic acid 1-[3,4-bis-(2,2,3,3,3-pentafluoro-propionyloxy)-phenyl]-2-[methyl-(2,2,3,3,3-pentafluoro-propionyl)-amino]-ethyl ester" is a complex organic molecule with a highly fluorinated structure. It features a pentafluoropropionic acid backbone, which is a three-carbon chain with five fluorine atoms. The compound includes a phenyl ring substituted at the 3,4-positions with two pentafluoropropionyloxy groups, and an ethyl ester group with a methyl group and a pentafluoropropionyl-amino group attached to the nitrogen. This molecule is characterized by its extensive fluorination, which can confer unique chemical and physical properties, such as increased lipophilicity and stability. The specific arrangement of fluorine atoms and functional groups in 2,2,3,3,3-Pentafluoro-propionic acid 1-[3,4-bis-(2,2,3,3,3-pentafluoro-propionyloxy)-phenyl]-2-[methyl-(2,2,3,3,3-pentafluoro-propionyl)-amino]-ethyl ester suggests potential applications in areas where such properties are beneficial, such as in pharmaceuticals or materials science.

1995-97-7

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1995-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1995-97-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1995-97:
(6*1)+(5*9)+(4*9)+(3*5)+(2*9)+(1*7)=127
127 % 10 = 7
So 1995-97-7 is a valid CAS Registry Number.

1995-97-7Downstream Products

1995-97-7Relevant academic research and scientific papers

Simultaneous profiling of multiple neurochemical pathways from a single cerebrospinal fluid sample using GC/MS/MS with electron capture detection

Eckstein, James A.,Ammerman, Gina M.,Reveles, Jessica M.,Ackermann, Bradley L.

experimental part, p. 782 - 790 (2009/04/07)

Biogenic amines and amino acids are widely characterized in the pathways representing neurotransmission. Although several analytical methodologies have been used to detect specific target molecules in relevant fluids such as cerebrospinal fluid (CSF), multiple assays must be used to survey the primary pathways involved. This article describes the development of a GC/MS/MS method capable of analyzing up to 43 analytes (representing 20 amino acids and more than seven neurochemical pathways) from a single 50 μl CSF sample. In this procedure, a CSF sample is first treated with acetonitrile to precipitate proteins. The dried sample is then derivatized with a mixture of 2,2,3,3,3-pentafluoro-1-propanol and pentafluoropropionic acetic anhydride to replace all active hydrogen atoms with fluorine-containing groups. Due to the concentration difference between amino acids and neurotransmitters, these two compound classes are analyzed in separate injections of the same derivatized extract. The total run time for each injection is approximately 15-20 min. An essential feature of the method is the use of argon as a reagent gas for electron capture chemical ionization (ECCI), as the use of the more traditional gas (methane) lacked sufficient durability to be considered for use with the present instrumentation. This article describes the development of this method including a detailed investigation of the chemical ionization conditions used. The resultant conditions allow for the profiling of biogenic amines (e.g. serotonin, norepinephrine, and dopamine) in the low picogram per milliliter range. Copyright

QUANTITATIVE MEASUREMENT OF OCTOPAMINES AND SYNEPHRINES IN URINE USING CAPILLARY COLUMN GAS CHROMATOGRAPHY NEGATIVE ION CHEMICAL IONIZATION MASS SPECTROMETRY.

Ibrahim,Couch,Williams,Budd,Yost,Midgley

, p. 1695 - 1699 (2007/10/02)

The isomeric octopamines and synephrines were measured in urine by a new assay which combines ion-exchange chromatography, capillary column gas chromatography, and electron capture negative ion chemical ionization mass spectrometry. Deuterium labeled anal

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