101527-53-1 Usage
Chemical structure
A complex organic molecule with a pyrimidine-2,4(1H,3H)-dione core structure.
Iodine atoms
Contains two iodine atoms in the molecule.
Hydroxy group
Features a hydroxy group attached to a propan-2-yl group.
Propan-2-yl group
The hydroxy group is attached to a propan-2-yl group, which is a three-carbon chain with a hydroxy group at the second carbon.
Ethyl group
Contains an ethyl group with a hydroxy group and an iodine atom attached to it.
Biological and pharmacological activity
The chemical structure suggests potential biological and pharmacological activity.
Research interest
May be of interest for further research in the fields of medicinal chemistry and drug development.
Experimental studies
The compound's precise properties and potential applications would need to be investigated through experimental studies.
Check Digit Verification of cas no
The CAS Registry Mumber 101527-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,5,2 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 101527-53:
(8*1)+(7*0)+(6*1)+(5*5)+(4*2)+(3*7)+(2*5)+(1*3)=81
81 % 10 = 1
So 101527-53-1 is a valid CAS Registry Number.
101527-53-1Relevant articles and documents
The Chemistry of 2',3'-Seconucleosides. 1. Synthesis and Chemical and Biological Properties of Derivatives of 2',3'- Secouridine
Jones, A. Stanley,Walker, Richard T.,Wyatt, Paul G.,Balzarini, Jan,Clercq, Erik De
, p. 3520 - 3532 (2007/10/02)
Aspects of the chemistry of 2',3'-secouridine (1-(R)-1,5-dihydroxy-4-hydroxymethyl-3-oxapent-2-yl)uracil) derivatives have been studied. 5'-O-Trityl-2',3'-secouridine (4) was obtained from 5'-O-trityluridine by oxidation with periodate followed by reducti
