326010-95-1 Usage
Uses
Used in Organic Synthesis:
3-Amino-1,1,1-trifluoro-5-methylhexan-2-ol is utilized as a reagent in organic synthesis, where its unique structural features facilitate the creation of a range of chemical products. Its trifluoromethyl group and amino functionality make it a key component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3-Amino-1,1,1-trifluoro-5-methylhexan-2-ol serves as a building block for the development of new drugs. Its chemical properties allow it to be incorporated into the molecular structures of potential therapeutic agents, enhancing their pharmacological profiles and contributing to the advancement of medicinal chemistry.
Used in Agrochemical Development:
3-Amino-1,1,1-trifluoro-5-methylhexan-2-ol is also employed in the agrochemical sector, where it is used as a precursor in the synthesis of various agrochemicals. Its lipophilic nature and reactivity make it suitable for the development of compounds with applications in crop protection and pest management.
Safety Considerations:
When handling 3-Amino-1,1,1-trifluoro-5-methylhexan-2-ol, it is crucial to implement appropriate safety measures to prevent exposure and potential harm. This includes the use of personal protective equipment, proper storage conditions, and adherence to guidelines for the safe disposal of chemical waste.
Check Digit Verification of cas no
The CAS Registry Mumber 326010-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,6,0,1 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 326010-95:
(8*3)+(7*2)+(6*6)+(5*0)+(4*1)+(3*0)+(2*9)+(1*5)=101
101 % 10 = 1
So 326010-95-1 is a valid CAS Registry Number.
326010-95-1Relevant academic research and scientific papers
Diastereoselective synthesis of β-amino-α-(trifluoromethyl) alcohols from homochiral α-dibenzylamino aldehydes
Andres, Jose M.,Pedrosa, Rafael,Perez-Encabo, Alfonso
, p. 1558 - 1566 (2007/10/03)
Homochiral α-dibenzylamino aldehydes, prepared from the corresponding α-amino acids, react with trimethyl(trifluoromethyl)silane in THF at 0 °C to afford, in good yields and dr, β-amino-α-(trifluoromethyl) alcohols; anti diastereomers were formed as major products in the trifluoromethylation reaction whereas syn diastereomers were obtained as single isomers in a two-step procedure. Swern oxidation of the mixtures formed in the trifluoromethylation leads to the corresponding α-dibenzylamino trifluoromethyl ketones which undergo diastereoselective reduction with sodium borohydride. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
