6708-06-1 Usage
Description
(5aS)-2,3,5aβ,6,7,8-Hexahydro-1H,5H-dipyrrolo[1,2-a:1',2'-d]pyrazine-5,10(10aβH)-dione is a complex organic compound with a unique molecular structure. It is characterized by its hexahydro-dipyrrolo-pyrazine framework, which may have potential applications in various fields due to its specific chemical properties.
Uses
Used in Pharmaceutical Industry:
(5aS)-2,3,5aβ,6,7,8-Hexahydro-1H,5H-dipyrrolo[1,2-a:1',2'-d]pyrazine-5,10(10aβH)-dione is used as an intermediate compound for the synthesis of various pharmaceutical agents. Its unique structure may contribute to the development of new drugs with specific therapeutic properties.
Used in Chemical Research:
In the field of chemical research, (5aS)-2,3,5aβ,6,7,8-Hexahydro-1H,5H-dipyrrolo[1,2-a:1',2'-d]pyrazine-5,10(10aβH)-dione can be utilized as a starting material or a building block for the creation of more complex molecules with potential applications in various industries.
Used in Material Science:
(5aS)-2,3,5aβ,6,7,8-Hexahydro-1H,5H-dipyrrolo[1,2-a:1',2'-d]pyrazine-5,10(10aβH)-dione may also find use in material science, where its unique properties could be exploited to develop new materials with specific characteristics, such as improved stability or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 6708-06-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6708-06:
(6*6)+(5*7)+(4*0)+(3*8)+(2*0)+(1*6)=101
101 % 10 = 1
So 6708-06-1 is a valid CAS Registry Number.
6708-06-1Relevant articles and documents
PdPb-Catalyzed decarboxylation of proline to pyrrolidine: Highly selective formation of a biobased amine in water
Verduyckt, Jasper,Van Hoof, Maarten,De Schouwer, Free,Wolberg, Marike,Kurttepeli, Mert,Eloy, Pierre,Gaigneaux, Eric M.,Bals, Sara,Kirschhock, Christine E.A.,De Vos, Dirk E.
, p. 7303 - 7310 (2018/05/23)
Amino acids have huge potential as platform chemicals in the biobased industry. Pd-catalyzed decarboxylation is a very promising route for the valorization of these natural compounds derived from protein waste or fermentation. We report that the highly abundant and nonessential amino acid L-proline is very reactive in the Pd-catalyzed decarboxylation. Full conversions are obtained with Pd/C and different Pd/MeOx catalysts; this allowed the identification of the different side reactions and the mapping of the reaction network. Due to the high reactivity of pyrrolidine, the selectivity for pyrrolidine was initially low. By carefully modifying Pd/ZrO2 with Pb in a controlled mannervia two incipient wetness impregnation stepsthe selectivity increased remarkably. Finally, a thorough investigation of the reaction parameters resulted in an increased activity of this modified catalyst and an even further enhanced selectivity under a low H2 pressure of 4 bar at 235 °C in water. This results in a very selective and sustainable production route for the highly interesting pyrrolidine.
