1250884-66-2 Usage
Uses
Used in Pharmaceutical Industry:
3-Boc-6-Amino-3-azabicyclo[3.2.0]heptane is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and functional groups allow for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 3-Boc-6-Amino-3-azabicyclo[3.2.0]heptane serves as a versatile building block for the preparation of a wide range of biologically active molecules. Its amino and Boc protecting group enable various chemical reactions, facilitating the synthesis of complex organic compounds.
Used in Research and Development:
3-Boc-6-Amino-3-azabicyclo[3.2.0]heptane is utilized in research and development for the exploration of new chemical reactions and the discovery of novel biologically active molecules. Its unique structure and functional groups provide opportunities for innovative synthetic strategies and the development of new chemical entities with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1250884-66-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,0,8,8 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1250884-66:
(9*1)+(8*2)+(7*5)+(6*0)+(5*8)+(4*8)+(3*4)+(2*6)+(1*6)=162
162 % 10 = 2
So 1250884-66-2 is a valid CAS Registry Number.
1250884-66-2Relevant articles and documents
Photocycloaddition of N-Benzylmaleimide to Alkenes As an Approach to Functional 3-Azabicyclo[3.2.0]heptanes
Skalenko, Yevhen A.,Druzhenko, Tetiana V.,Denisenko, Aleksandr V.,Samoilenko, Maryna V.,Dacenko, Oleksandr P.,Trofymchuk, Serhii A.,Grygorenko, Oleksandr O.,Tolmachev, Andrey A.,Mykhailiuk, Pavel K.
, p. 6275 - 6289 (2018)
A one-step synthesis of functionalized 3-azabicyclo[3.2.0]heptanes by [2+2]-photochemical intermolecular cycloaddition of N-benzylmaleimide to alkenes was elaborated. The obtained compounds were easily transformed into the bi- and tricyclic analogues of piperidine, morpholine, piperazine, and GABA, which are advanced building blocks for drug discovery.
