97931-41-4 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 3-carbazolecarboxylate is used as an intermediate in the synthesis of pharmaceuticals for its antiviral, antifungal, and antitumor properties. Its biological activities make it a valuable component in the development of new drugs targeting a range of health conditions.
Used in Dye Industry:
In the dye industry, Methyl 3-carbazolecarboxylate is utilized as a key intermediate in the production of various dyes. Its chemical structure contributes to the color and stability of the dyes, enhancing their performance in different applications.
Used in Organic Electronics:
Methyl 3-carbazolecarboxylate is used as a component in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and electroluminescent devices. Its light-emitting properties make it a promising material for creating efficient and eco-friendly electronic displays and lighting solutions.
Used in Pesticide Production:
As an intermediate in the production of pesticides, Methyl 3-carbazolecarboxylate contributes to the development of effective and targeted pest control solutions, helping to protect crops and maintain agricultural productivity.
Used in Fluorescent Brightener and UV Stabilizer Production:
Methyl 3-carbazolecarboxylate is also used in the synthesis of fluorescent brighteners and UV stabilizers. Its chemical properties enhance the performance of these additives, improving the durability and appearance of various materials and products.
Check Digit Verification of cas no
The CAS Registry Mumber 97931-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,3 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97931-41:
(7*9)+(6*7)+(5*9)+(4*3)+(3*1)+(2*4)+(1*1)=174
174 % 10 = 4
So 97931-41-4 is a valid CAS Registry Number.
97931-41-4Relevant academic research and scientific papers
Synthesis of substituted carbazoles via electrocyclization of in situ generated enamines from 1-phenylsulfonyl-2/(3)-methyl-3/(2)-vinylindoles and DMF·DMA/DMA·DMA
Sureshbabu, Radhakrishnan,Balamurugan, Ramalingam,Mohanakrishnan, Arasambattu K.
scheme or table, p. 3582 - 3591 (2009/09/08)
Interaction of 2/(3)-methyl-3/(2)-vinylindoles and DMF·DMA/DMA·DMA at 110 °C led to the in situ generation of enamines, which on concurrent electrocyclization followed by subsequent aromatization afforded substituted carbazoles.
A novel synthesis of N-protected carbazoles involving electrocyclization of in situ generated enamines
Mohanakrishnan, Arasambattu K.,Balamurugan, Ramalingam
, p. 4045 - 4048 (2007/10/03)
A new route for the synthesis of carbazoles has been realized through the intermediacy of 2,3-divinylindoles involving an electrocyclization followed by aromatization.
Regiochemical switching in Diels-Alder cycloadditions by change in oxidation state of removable diene sulfur substituents. Synthesis of carbazoles by sequential heteroannulation and Diels-Alder cycloaddition
Back, Thomas G.,Pandyra, Aleksandra,Wulff, Jeremy E.
, p. 3299 - 3302 (2007/10/03)
The palladium-catalyzed heteroannulation of N-carbobenzyloxy-o-iodoanilines with 1-phenylthio-1,3-butadiene afforded indolines 7, which were oxidized with DDQ to produce vinylogous 2-(phenylthio)indoles 8. The latter compounds underwent highly regioselect
