140226-10-4 Usage
Explanation
Represents the total number of atoms of each element present in the compound.
Explanation
Describes the physical appearance of the compound in its solid state.
Explanation
Indicates the spatial arrangement of the atoms in the molecule, specifically the configuration at the 2nd, 4th, and 5th carbon atoms.
Explanation
Identifies the specific functional groups present in the compound, which contribute to its chemical properties and reactivity.
Explanation
Suggests the possible biological activities of the compound, which can be further studied for medical applications.
Explanation
Provides an alternative name for the compound, which is less commonly used in scientific literature.
Appearance
White to off-white solid
Stereochemistry
(2R,4S,5R)
Functional groups
Azido, hydroxymethyl, methoxytetrahydrofuran, and pyrimidine-2,4-dione
Potential properties
Antiviral and antitumor
Research and pharmaceutical applications
Used in research and pharmaceutical applications
Check Digit Verification of cas no
The CAS Registry Mumber 140226-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,2,2 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 140226-10:
(8*1)+(7*4)+(6*0)+(5*2)+(4*2)+(3*6)+(2*1)+(1*0)=74
74 % 10 = 4
So 140226-10-4 is a valid CAS Registry Number.
140226-10-4Relevant academic research and scientific papers
Synthesis and anti-HIV activity of 4'-azido- and 4'-methoxynucleosides
Maag,Rydzewski,McRoberts,Crawford-Ruth,Verheyden,Prisbe
, p. 1440 - 1451 (2007/10/02)
A series of nucleosides were synthesized in which the 4'-hydrogen was substituted with either an azido or a methoxy group. The key steps in the syntheses of the 4'-azido analogues were the stereo- and regioselective addition of iodine azide to a 4'-unsatu
