131544-74-6 Usage
Chemical structure
A cyclopropane ring with two phenyl groups and a 4-methoxyphenyl group attached, along with two chlorine atoms.
Complexity
The compound has a complex structure due to the presence of multiple functional groups and aromatic rings.
Reactivity
High reactivity, making it useful in the production of various pharmaceuticals and other organic compounds.
Pharmaceutical industry
Used for the synthesis of drugs and other biologically active molecules.
Organic synthesis
Utilized as a building block in the preparation of a wide range of organic compounds.
Chemical reactions
Capable of undergoing various chemical reactions due to its unique structure and functional groups.
Functional groups
Contains a cyclopropane ring, phenyl groups, a 4-methoxyphenyl group, and chlorine atoms.
Stability
The compound's stability may vary depending on the reaction conditions and the presence of other reactants.
Solubility
The solubility of the compound in different solvents can be influenced by its polarity and the presence of functional groups.
Purity
The purity of the compound can affect its reactivity and the yield of the desired product in chemical reactions.
Safety
As with any chemical compound, proper handling and storage are essential to ensure safety during its use in research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 131544-74-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,5,4 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131544-74:
(8*1)+(7*3)+(6*1)+(5*5)+(4*4)+(3*4)+(2*7)+(1*4)=106
106 % 10 = 6
So 131544-74-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H18Cl2O/c1-25-19-14-12-18(13-15-19)21(17-10-6-3-7-11-17)20(22(21,23)24)16-8-4-2-5-9-16/h2-15,20H,1H3
131544-74-6Relevant articles and documents
Synthesis and chiral separation of some antitumor agents
Singh, Satendra,Meyer, Karen L.,Magarian, Robert A.
, p. 81 - 94 (2007/10/03)
Four Z-isomers of 1,1-dichloro-2,2,3-triarylcyclopropane (DTACs), designed as potent antitumor agents, were synthesized from their appropriately substituted ethenes, which were prepared from the Grignard reaction followed by the dehydration of their inter
