6340-71-2 Usage
Chemical class
Belongs to the class of piperidine compounds.
Structure
Composed of a bicyclo[2.2.1]hept-2-ylcarbonyl group attached to a 4-methylpiperidine ring.
Potential applications
Has potential applications in the field of organic chemistry and pharmaceuticals.
Usage
May be used as a building block in the synthesis of various organic compounds and pharmaceutical drugs.
Structural features
Distinct structural features make it a valuable intermediate in chemical synthesis and medicinal chemistry.
Development and exploration
Has potential for further development and exploration in various scientific and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6340-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6340-71:
(6*6)+(5*3)+(4*4)+(3*0)+(2*7)+(1*1)=82
82 % 10 = 2
So 6340-71-2 is a valid CAS Registry Number.
6340-71-2Relevant academic research and scientific papers
Chemo- and diastereoselective reduction of β-enamino esters: A convenient synthesis of both cis- and trans-γ-amino alcohols and β-amino esters
Bartoli,Cimarelli,Marcantoni,Palmieri,Petrini
, p. 5328 - 5335 (2007/10/02)
Convenient procedures for the chemo- and diastereoselective reduction of b-enamino esters 1 are described. Both cis- and trans-γ-amino alcohols 2 or b-amino esters 3 can be prepared by reduction of b-enamino esters 1, readily available starting materials, with the use of inexpensive reagents Na/i-PrOH or NaHB(OAc)3/AcOH, respectively, and the appropriate reduction conditions. The mechanisms and diastereoselectivities for the reductions are discussed. The relative configurations and conformations of the diastereoisomeric γ-amino alcohols 2 and β-amino esters 3 obtained are established by 1H and 13C NMR study and unequivocally set by their cyclic derivatives tetrahydro-1,3-oxazines 4.
