155322-95-5 Usage
General Description
Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-(hydroxymethyl)-, (3R-cis)- (9CI) is a chemical compound with a complex structure containing a pyrrolopyrazinedione core. It is a hexahydro derivative with a cis configuration and a hydroxymethyl group attached to the third carbon atom. Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-(hydroxymethyl)-, (3R-cis)- (9CI) has potential applications in medicinal chemistry and drug development due to its unique structure and potential pharmacological properties. It may also be used as a building block in organic synthesis for the preparation of novel molecules with biological activity. Further research is needed to fully understand its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 155322-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,3,2 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 155322-95:
(8*1)+(7*5)+(6*5)+(5*3)+(4*2)+(3*2)+(2*9)+(1*5)=125
125 % 10 = 5
So 155322-95-5 is a valid CAS Registry Number.
155322-95-5Relevant articles and documents
AGRICULTURAL CHEMICAL CONTAINING 2,5-DIKETOPIPERAZINE DERIVATIVE AS ACTIVE INGREDIENT
-
Paragraph 0033, (2013/06/05)
Disclosed herein is an agricultural agent containing a 2,5-diketopiperazine derivative capable of controlling plant diseases and promoting plant growth or an agriculturally acceptable salt thereof as an active ingredient.
Chiral Ligands Containing Heteroatoms. 11. Optically Active 2-Hydroxymethyl Piperazines as Catalyst in the Enantioselective Addition of Diethylzinc to Benzaldehyde
Falorni, Massimo,Satta, Michele,Conti, Sandra,Giacomelli, Giampaolo
, p. 2389 - 2398 (2007/10/02)
Starting from enantiomerically pure serine, a series of (2R,5S) and (2S,5S)-2-hydroxymethyl-5-alkyl piperazines 1-5 were prepared in good yields without any racemization.The use of these compounds as chiral catalysts for the enantioselective addition of d