195737-40-7 Usage
Chemical structure
The compound consists of multiple connected phenyl rings with several methoxy groups attached.
Number of phenyl rings
The compound has a total of seven phenyl rings.
Number of methoxy groups
The compound has a total of seven methoxy groups.
Industrial applications
The compound is commonly used in various industrial applications, such as in the production of polymers, plastics, and other materials.
Complex and large molecule
The compound is a complex and large molecule due to its multiple connected phenyl rings and methoxy groups.
Specific properties and uses
The specific properties and uses of this compound can vary depending on the exact structure and arrangement of its components.
Substitution pattern
The compound has a specific substitution pattern of methoxy groups on the phenyl rings, which can affect its properties and applications.
Solubility
The compound's solubility can be influenced by the presence of methoxy groups, which can increase its solubility in certain solvents.
Stability
The compound's stability can be affected by the arrangement of its phenyl rings and methoxy groups, which can impact its reactivity and shelf life.
Synthesis
The synthesis of this compound can be complex and may require multiple steps, depending on the specific structure and arrangement of its components.
Check Digit Verification of cas no
The CAS Registry Mumber 195737-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,7,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 195737-40:
(8*1)+(7*9)+(6*5)+(5*7)+(4*3)+(3*7)+(2*4)+(1*0)=177
177 % 10 = 7
So 195737-40-7 is a valid CAS Registry Number.
195737-40-7Relevant articles and documents
p-octiphenyl β-barrels with ion channel and esterase activity
Baumeister, Bodo,Sakai, Naomi,Matile, Stefan
, p. 4229 - 4232 (2007/10/03)
(Metrix Presented) Design, synthesis, and esterase and ion channel activity of a novel barrel-stave supramolecule with hydrophobic exterior and histidine-rich interior are reported. Voltage-dependent binding of pyrenyl-8-oxy-1,3,6-trisulfonates by histidi