170033-58-6 Usage
General Description
Tert-butyl-4-benzyl-2(R)-methyl-piperazinecarboxylate is a chemical compound with the molecular formula C22H32N2O2. It is a piperazine derivative containing a tert-butyl group, a benzyl group, and a methyl group. This chemical is often used as an intermediate in the synthesis of pharmaceutical compounds and agrochemicals. It may also have potential applications in medicinal chemistry and drug discovery due to its structural features and potential biological activities. Additionally, tert-butyl-4-benzyl-2(R)-methyl-piperazinecarboxylate may be used as a building block in organic synthesis for the creation of novel chemical entities with diverse properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 170033-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,0,3 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 170033-58:
(8*1)+(7*7)+(6*0)+(5*0)+(4*3)+(3*3)+(2*5)+(1*8)=96
96 % 10 = 6
So 170033-58-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H26N2O2/c1-14-12-18(13-15-8-6-5-7-9-15)10-11-19(14)16(20)21-17(2,3)4/h5-9,14H,10-13H2,1-4H3/t14-/m1/s1
170033-58-6Relevant 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
A novel and facile method to synthesize (R)- and (S)-2-methylpiperazine
Liu, Bo,Xu, Guang-Yu,Yang, Chun-Hao,Wu, Xi-Han,Xie, Yu-Yuan
, p. 4111 - 4118 (2007/10/03)
A concise and efficient synthesis of (R)- and (S)-2-methylpiperazine in only five steps from (D)- and (L)-alanine is described. The key step is reaction of benzylamine with a bifunctional molecule to build a six-membered ring.
Imidazo[1,5-A]quinolines for treatment of anxiety and sleep disorders
-
, (2008/06/13)
Imidazo[1,5-a]quinolines of formula (I) which are useful pharmaceutical agents for the treatment of anxiety, sleep disorders, panic states, convulsions and muscle disorders. STR1