130432-39-2 Usage
General Description
"(S)-2-Amino-3-methyl-1,1-diphenyl-1-butanol" is a chemical compound that belongs to the group of amino alcohols. This complex organic molecule features an amino group (-NH2), two phenyl ring structures, a secondary alcohol group (-OH), and a methyl group (-CH3). The "(S)-" prefix in its name signifies that it has a specific configuration in chiral (asymmetric) carbon atoms according to the Cahn-Ingold-Prelog priority rules, meaning it only rotates the plane-polarized light in one direction. While this compound's exact functional uses are not commonly detailed in general resources, amino alcohols such as this one are often used in the synthesis of pharmaceuticals, and as intermediates in organic synthesis. Its physical and chemical properties, safety, handling instructions, and potential risks would usually be provided in a safety data sheet by suppliers.
Check Digit Verification of cas no
The CAS Registry Mumber 130432-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,3 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130432-39:
(8*1)+(7*3)+(6*0)+(5*4)+(4*3)+(3*2)+(2*3)+(1*9)=82
82 % 10 = 2
So 130432-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H21NO.ClH/c1-13(2)16(18)17(19,14-9-5-3-6-10-14)15-11-7-4-8-12-15;/h3-13,16,19H,18H2,1-2H3;1H/t16-;/m0./s1
130432-39-2Relevant articles and documents
Ethynylbenziodoxolones (EBX) as reagents for the ethynylation of stabilized enolates
Fernandez Gonzalez, Davinia,Brand, Jonathan P.,Mondiere, Regis,Waser, Jerome
supporting information, p. 1631 - 1639 (2013/07/05)
Herein, we report a detailed study on the electrophilic alkynylation of cyclic keto esters and amides with ethynylbenziodoxolone (EBX) reagents. The structure and stability of this class of reagents is first described more in details. Differential scannin
Synthesis of chiral tetraaminophosphonium chlorides from N-Boc α-amino acid esters
Uraguchi, Daisuke,Sakaki, Sawako,Ueki, Yusuke,Ito, Takaki,Ooi, Takashi
scheme or table, p. 1081 - 1085 (2009/06/28)
Preparation of chiral tetraaminophosphonium chlorides of type 1 starting from N-Boc α-amino acid esters is described. Modified conditions for the displacement of the tertiary hydroxy group of the intermediary amino alcohol pave a way for the assembly of 1