908338-20-5 Usage
Description
(R)-3-(2-(Aminomethyl)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-9-yl)-4-(phenylamino)-1H-pyrrole-2,5-dione methanesulfonate is a complex dihydroindolone derivative featuring a pyrroloindolone core structure with an aminomethyl group and a phenylamino group attached. (R)-3-(2-(Aminomethyl)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-9-yl)-4-(phenylamino)-1H-pyrrole-2,5-dione methanesulfonate, in the form of a methanesulfonate salt, is utilized as a chemical intermediate in the synthesis of pharmaceutical compounds. Its unique structure and properties render it valuable for a range of chemical and pharmaceutical applications, particularly in drug development and research.
Uses
Used in Pharmaceutical Industry:
(R)-3-(2-(Aminomethyl)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-9-yl)-4-(phenylamino)-1H-pyrrole-2,5-dione methanesulfonate is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Drug Development:
In the field of drug development, this compound serves as a valuable building block for creating novel molecules with specific biological activities. Its incorporation into drug candidates can lead to the discovery of new treatments for various diseases and conditions.
Used in Research:
(R)-3-(2-(Aminomethyl)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-9-yl)-4-(phenylamino)-1H-pyrrole-2,5-dione methanesulfonate is also used in research settings to study the interactions between its molecular structure and biological targets. This understanding can help in the design and optimization of more effective drugs.
Used in Chemical Synthesis:
(R)-3-(2-(Aminomethyl)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-9-yl)-4-(phenylamino)-1H-pyrrole-2,5-dione methanesulfonate is employed in chemical synthesis processes, where its unique functional groups can be utilized to create a variety of new molecules with different properties and applications. This can lead to the development of new materials, catalysts, or other chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 908338-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,3,3 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 908338-20:
(8*9)+(7*0)+(6*8)+(5*3)+(4*3)+(3*8)+(2*2)+(1*0)=175
175 % 10 = 5
So 908338-20-5 is a valid CAS Registry Number.
908338-20-5Relevant articles and documents
One-step synthesis of heteroaromatic-fused pyrrolidines via cyclopropane ring-opening reaction: Application to the PKCβ inhibitor JTT-010
Tanaka, Masahiro,Ubukata, Minoru,Matsuo, Takafumi,Yasue, Katsutaka,Matsumoto, Katsuya,Kajimoto, Yasuyuki,Ogo, Takashi,Inaba, Takashi
, p. 3331 - 3334 (2008/02/11)
A ring-opening reaction of cyclopropanes with five-membered heteroaromatics having a leaving group at C(2) was found to provide heteroaromatic-fused pyrrolidines in one step. This reaction was successfully applied to the synthesis of the protein kinase C-β inhibitor JTT-010, which possesses a dihydropyrrolo[1,2-a]indole core.
