131266-15-4 Usage
Functionality
Used as an intermediate in the synthesis of pharmaceuticals and other organic compounds
Structure
A diacetate ester of a 1,3-Propanediol derivative containing a purinyl moiety
Biological Activity
Has potential biological activity and is used in research and development of new drugs
Safety Precautions
Important to handle with care and follow safety protocols due to potential health hazards
Applications
Widely used in the pharmaceutical industry for the development of new drugs
Molecular Weight
330.31 g/mol
Appearance
Colorless to white crystalline solid
Solubility
Soluble in organic solvents like methanol, ethanol, and dimethyl sulfoxide (DMSO)
Stability
Stable under normal temperature and pressure, but sensitive to moisture and light
Storage
Should be stored in a cool, dry, and well-closed container, protected from light and moisture
Hazardous Classification
Classified as a hazardous substance due to its potential health risks
Regulatory Information
Follow local and international regulations for handling, storage, and disposal of hazardous chemicals
Disposal
Dispose of in accordance with local regulations and guidelines for hazardous waste management
Check Digit Verification of cas no
The CAS Registry Mumber 131266-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,6 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 131266-15:
(8*1)+(7*3)+(6*1)+(5*2)+(4*6)+(3*6)+(2*1)+(1*5)=94
94 % 10 = 4
So 131266-15-4 is a valid CAS Registry Number.
131266-15-4Relevant articles and documents
PROCESS FOR PREPARING 9-[4-ACETOXY-3-(ACETOXYMETHYL)BUT-1-YL]-2-AMINOPURINE
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Page 9-11, (2008/06/13)
Disclosed is a process for preparing 9-[4-acetoxy-3-(acetoxymethyl)but-1-yl]-2-aminopurine (called Famciclovir), a drug of purine derivatives having antiviral activity. This process comprises reacting 2-aminopurine with 2-acetoxymethyl-4-bromobut-1-yl-acetate in the presence of thallium (I) ethoxide to give the desired compound. According to this process, the desired compound can be prepared in very high selectivity and purity under mild reaction conditions.