326010-95-1 Usage
General Description
3-Amino-1,1,1-trifluoro-5-methylhexan-2-ol is a chemical compound that belongs to the class of alcohols and amines. It is a clear, colorless liquid with a molecular formula C7H14F3NO. 3-Amino-1,1,1-trifluoro-5-methylhexan-2-ol is mainly used as a reagent in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals. It possesses a trifluoromethyl group, which makes it highly lipophilic and can increase its stability against metabolism in living organisms. Additionally, the amino group can participate in various chemical reactions, making it a versatile and valuable compound in chemical research and development. Safety precautions should be taken when handling this chemical, as it may present hazards to human health and the environment if not properly managed.
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 articles and documents
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.
