914223-46-4 Usage
Description
3-AMINO-4,4,4-TRIFLUORO-BUTAN-1-OL, also known as trifluoroisobutanolamine, is a colorless liquid with a strong odor, featuring a trifluoromethyl group and an amino group. It is a compound with the chemical formula C4H8F3NO, commonly used in organic synthesis and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
3-AMINO-4,4,4-TRIFLUORO-BUTAN-1-OL is used as a building block in the synthesis of various pharmaceutical compounds due to its unique trifluoromethyl and amino functional groups.
Used in Agrochemicals:
3-AMINO-4,4,4-TRIFLUORO-BUTAN-1-OL is used as a precursor in the synthesis of agrochemicals, contributing to the development of new and effective crop protection agents.
Used in Specialty Chemicals:
3-AMINO-4,4,4-TRIFLUORO-BUTAN-1-OL is used as a key intermediate in the production of specialty chemicals, enabling the creation of innovative and high-performance materials.
Used in Fluorinated Compounds:
3-AMINO-4,4,4-TRIFLUORO-BUTAN-1-OL is used in the production of fluorinated compounds, which have a wide range of applications in various industries, including pharmaceuticals, materials science, and agrochemicals.
Used as a Solvent in Chemical Reactions:
3-AMINO-4,4,4-TRIFLUORO-BUTAN-1-OL is used as a solvent in various chemical reactions, facilitating the synthesis of target compounds and improving reaction efficiency.
Check Digit Verification of cas no
The CAS Registry Mumber 914223-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,2,2 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 914223-46:
(8*9)+(7*1)+(6*4)+(5*2)+(4*2)+(3*3)+(2*4)+(1*6)=144
144 % 10 = 4
So 914223-46-4 is a valid CAS Registry Number.
914223-46-4Relevant articles and documents
Ethyl-4,4,4-trifluoroacetoacetate (ETFAA), a powerful building block for enantiopure chirons in trifluoromethyl-β-amino acid series
Michaut, Valérie,Metz, Fran?ois,Paris, Jean-Marc,Plaquevent, Jean-Christophe
, p. 889 - 895 (2008/03/14)
Herein are studied new transformations of ethyl-4,4,4-trifluoroacetoacetate (ETFAA), giving access to a series of enantiopure chirons bearing both a trifluoromethyl group and an amino moiety. The key intermediate is obtained optically pure by a resolution
