33245-77-1 Usage
Functional groups
Chloro group, Ketone functional group, 3,4-dimethoxyphenyl group
Structure
Contains a 5-oxopentane chain with a chlorinated carbon at the 1st position and a 3,4-dimethoxyphenyl group attached to the 5th position
Applications
Organic synthesis, Pharmaceutical research
Health and safety hazards
Potential health and safety risks, proper precautions required for handling
Physical state
Likely a liquid or solid at room temperature (not specified in the material)
Solubility
Not specified in the material, but may be soluble in organic solvents due to its nonpolar nature
Reactivity
Reactive towards nucleophiles due to the presence of the electrophilic chloro and ketone groups
Stability
Stable under normal conditions, but sensitive to heat, light, or strong bases/acids (not specified in the material)
Synthesis
Not specified in the material, but may involve the reaction of a 5-oxopentane derivative with a 3,4-dimethoxyphenyl chloride or a similar electrophile
Check Digit Verification of cas no
The CAS Registry Mumber 33245-77-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,4 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33245-77:
(7*3)+(6*3)+(5*2)+(4*4)+(3*5)+(2*7)+(1*7)=101
101 % 10 = 1
So 33245-77-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H17ClO3/c1-16-12-7-6-10(9-13(12)17-2)11(15)5-3-4-8-14/h6-7,9H,3-5,8H2,1-2H3
33245-77-1Relevant academic research and scientific papers
Synthesis and some properties of 6-(ω-aroylbutylthio)purines
Gromov,Skachilova,Aleksandrova,Kochergin
, p. 1225 - 1229 (2007/10/03)
A series of 6-(ω-aroylthio)purines, which have not been described in the literature, has been obtained by the reaction of 6-purinethione with ω-chlorovalerophenone and its substituted derivatives. Some properties of the compounds synthesized have been studied, viz. reaction at the carbonyl group, methylation, and hydrolysis. 1999 KluwerAcademic/Plenum Publishers.
