796096-64-5 Usage
General Description
(S)-1-N-Boc-piperazine-2-carboxylic acid methyl ester is a chemical compound that is used in pharmaceutical research and drug development. It belongs to the class of piperazine derivatives and has a methyl ester functional group. (S)-1-N-Boc-piperazine-2-carboxylic acid methyl ester is known for its potential as a building block in the synthesis of various bioactive compounds and drug candidates. It has been studied for its potential biological activities and pharmacological properties, making it a valuable molecule in the field of medicinal chemistry. Additionally, its (S)-stereoisomer configuration makes it particularly interesting for certain applications. Overall, (S)-1-N-Boc-piperazine-2-carboxylic acid methyl ester is an important chemical compound with potential in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 796096-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,6,0,9 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 796096-64:
(8*7)+(7*9)+(6*6)+(5*0)+(4*9)+(3*6)+(2*6)+(1*4)=225
225 % 10 = 5
So 796096-64-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H20N2O4/c1-11(2,3)17-10(15)13-6-5-12-7-8(13)9(14)16-4/h8,12H,5-7H2,1-4H3/t8-/m0/s1
796096-64-5Relevant articles and documents
Synthesis of Enantiopure Piperazines via Asymmetric Lithiation-Trapping of N-Boc Piperazines: Unexpected Role of the Electrophile and Distal N-Substituent
Firth, James D.,O'Brien, Peter,Ferris, Leigh
, p. 651 - 659 (2016/01/29)
A new method for the synthesis of enantiopure α-substituted piperazines via direct functionalization of the intact piperazine ring is described. The approach utilizes the asymmetric lithiation-substitution of an α-methylbenzyl-functionalized N-Boc piperaz
