106674-01-5 Usage
Uses
Used in Organic Synthesis:
[3,3'-Bi-1H-pyrrole]-4,5'-dicarboxylic acid, 1'-[(4-methylphenyl)sulfonyl]-, 5'-methyl 4-(phenylmethyl) ester is used as a building block in organic synthesis for the creation of more complex molecules due to its diverse functional groups and aromatic rings.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [3,3'-Bi-1H-pyrrole]-4,5'-dicarboxylic acid, 1'-[(4-methylphenyl)sulfonyl]-, 5'-methyl 4-(phenylmethyl) ester is used as a potential candidate for drug development, given its unique structure and functional groups that can be tailored for specific therapeutic applications.
Used in Material Science:
[3,3'-Bi-1H-pyrrole]-4,5'-dicarboxylic acid, 1'-[(4-methylphenyl)sulfonyl]-, 5'-methyl 4-(phenylmethyl) ester is used as a precursor in the development of new materials, such as polymers or composites, due to its versatile chemical structure and potential for functionalization.
Used in Chemical Research:
In the chemical research industry, [3,3'-Bi-1H-pyrrole]-4,5'-dicarboxylic acid, 1'-[(4-methylphenyl)sulfonyl]-, 5'-methyl 4-(phenylmethyl) ester is used as a subject of study to explore its properties, reactivity, and potential applications in various chemical processes and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 106674-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,7 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106674-01:
(8*1)+(7*0)+(6*6)+(5*6)+(4*7)+(3*4)+(2*0)+(1*1)=115
115 % 10 = 5
So 106674-01-5 is a valid CAS Registry Number.
106674-01-5Relevant academic research and scientific papers
Studies on the Synthesis of the Antitumor Agent CC-1065. Synthesis of PDE I and PDE II, Inhibitors of Cyclic Adenosine-3',5'-monophosphate Phosphodiesterase Using the 3,3'-Bipyrrole Strategy
Carter, Paul,Fitzjohn, Steven,Halazy, Serge,Magnus, Philip
, p. 2711 - 2717 (2007/10/02)
In the model series tert-butyl 2,4-pentadienoate was treated with TosCHMeNC/NaH to give the pyrrole 18, which was converted into the 3,3'-bipyrrole 20.Treatment of the pyrrole 20 with oxalyl chloride gave the o-quinone 21, which was reduced and concomitan