80541-20-4 Usage
Chemical structure
1-(5-O-benzylpentofuranosyl)-1H-pyrrole is composed of a furanosyl and pyrrole moiety, with a benzyl group attached to the pentofuranosyl unit.
Aromatic properties
Due to the presence of a benzyl group, the compound is likely to exhibit aromatic characteristics.
Biological significance
The compound has potential biological activities and may be significant in the drug discovery process.
Pharmacological potential
It may have potential as a pharmacological agent, warranting further research to explore its therapeutic properties in various diseases.
Applications in organic synthesis
The compound may have uses in the field of organic synthesis for the development of novel compounds with desired properties.
Medicinal chemistry
It may also be utilized in medicinal chemistry for the development of new drugs and therapeutic agents.
Further research
Additional studies may be necessary to fully understand the compound's properties, potential applications, and therapeutic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 80541-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,4 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80541-20:
(7*8)+(6*0)+(5*5)+(4*4)+(3*1)+(2*2)+(1*0)=104
104 % 10 = 4
So 80541-20-4 is a valid CAS Registry Number.
80541-20-4Relevant articles and documents
THE REACTIONS OF BENZYLATED PYRROLE AND ADENINE RIBONUCLEOSIDES WITH GRIGNARD REAGENTS
Kawana, Masajiro
, p. 1541 - 1542 (2007/10/02)
The anomerization of benzylated pyrrole nucleosides were found to proceed by the use of t-BuMgBr.These nucleosides also reacted with MeMgI to produce open-chain products.On the other hand, the reaction of a perbenzylated adenosine with the Grignard reagen
