1026230-99-8 Usage
General Description
(S)-b-Amino-3-Methyl-benzeneethanol is a chemical compound with the molecular formula C9H13NO. It is an optically active compound, with a specific rotation of -43° to -46°. (S)-b-AMino-3-Methyl-benzeneethanol is commonly used as a chiral building block in the synthesis of various pharmaceuticals and organic compounds. It is also known for its role as an intermediate in the production of enantiomerically pure drugs and fine chemicals. In addition, (S)-b-Amino-3-Methyl-benzeneethanol has applications in the field of asymmetric synthesis and drug discovery, demonstrating its importance and versatility in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 1026230-99-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,2,3 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1026230-99:
(9*1)+(8*0)+(7*2)+(6*6)+(5*2)+(4*3)+(3*0)+(2*9)+(1*9)=108
108 % 10 = 8
So 1026230-99-8 is a valid CAS Registry Number.
1026230-99-8Relevant articles and documents
Diastereoselective and Enantiospecific Synthesis of 1,3-Diamines via 2-Azaallyl Anion Benzylic Ring-Opening of Aziridines
Li, Kangnan,Weber, Alexandria E.,Tseng, Luke,Malcolmson, Steven J.
supporting information, p. 4239 - 4242 (2017/08/23)
The 1,3-diamine motif appears in numerous complex molecules, yet there are few methods for the stereoselective construction of this moiety. Herein, we demonstrate a stereocontrolled synthesis of 1,3-diamines, which bear up to three contiguous stereogenic centers, through benzylic ring-opening of aziridines with 2-azaallyl anion nucleophiles. Reactions proceed efficiently (yield up to 95%), diastereoselectively (dr up to >20:1), site selectively, and enantiospecifically to deliver products with differentiated amino groups.
