28485-24-7 Usage
Chemical structure
A pyrimidine derivative with two benzyl groups attached to the 1st and 5th positions, and a carbonyl group at the 2nd and 4th positions.
Appearance
Typically a solid or crystalline compound.
Biological activities
Exhibits antiviral and anticancer properties.
Organic synthesis
Used as a building block in the synthesis of various pharmacologically active compounds.
Pharmaceutical research
Investigated for its potential therapeutic applications in medicinal and pharmaceutical fields.
Solubility
Soluble in organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO).
Stability
Generally stable under normal laboratory conditions, but sensitive to heat, light, and moisture.
Purity
Often synthesized with a high degree of purity for use in research and pharmaceutical applications.
Safety precautions
Handle with care, as it may have potential toxic effects. Use appropriate personal protective equipment (PPE) and follow proper disposal procedures.
Storage
Store in a cool, dry, and dark place, preferably in airtight containers to protect from light and moisture.
Check Digit Verification of cas no
The CAS Registry Mumber 28485-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,8 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28485-24:
(7*2)+(6*8)+(5*4)+(4*8)+(3*5)+(2*2)+(1*4)=137
137 % 10 = 7
So 28485-24-7 is a valid CAS Registry Number.
28485-24-7Relevant articles and documents
Sodium hydride mediated cascade reaction towards the synthesis of 1,5-disubstituted uracil from cyanamides derived from Baylis-Hillman adducts
Nag,Yadav,Maulik,Batra
, p. 911 - 917 (2007/12/27)
The substituted cyanamides generated from Baylis-Hillman adducts afford 1,5-disubstituted uracils via a sodium hydride induced cascade reaction involving sequential intramolecular attack of the hydroxy group on the nitrile group, cyclization of the result