3998-04-7 Usage
Description
9-Allylcarbazole, with the molecular formula C14H13N, is a chemical compound derived from carbazole, featuring both an allyl and a carbazole group. It is known for its applications across various domains such as organic synthesis, materials science, and pharmaceutical research, where it serves as a building block for organic compounds and a monomer for polymer production. Its electronic and photophysical properties also make it a candidate for optoelectronic devices like organic light-emitting diodes (OLEDs). Furthermore, it has been explored for potential biological activities and therapeutic properties within the pharmaceutical industry.
Uses
Used in Organic Synthesis:
9-Allylcarbazole is used as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Materials Science:
In the field of materials science, 9-allylcarbazole is utilized as a monomer for the production of polymers, which can be engineered for specific material properties and uses.
Used in Optoelectronic Devices:
9-Allylcarbazole is used as a component in the development of optoelectronic devices, particularly organic light-emitting diodes (OLEDs), due to its beneficial electronic and photophysical characteristics.
Used in Pharmaceutical Research:
Within the pharmaceutical industry, 9-allylcarbazole is studied for its potential biological activities and therapeutic properties, indicating its possible use in the discovery and development of new drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 3998-04-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,9 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3998-04:
(6*3)+(5*9)+(4*9)+(3*8)+(2*0)+(1*4)=127
127 % 10 = 7
So 3998-04-7 is a valid CAS Registry Number.
3998-04-7Relevant articles and documents
Design, synthesis and antifungal activity of carbazole derivatives
Zhu, Shi-Ping,Wang, Wen-Ya,Fang, Kun,Li, Zheng-Gang,Dong, Guo-Qiang,Miao, Zhen-Yuan,Yao, Jian-Zhong,Zhang, Wan-Nian,Sheng, Chun-Quan
, p. 229 - 233 (2014/02/14)
The incidence of invasive fungal infections is increasing rapidly. Clinically available antifungal agents suffer from limited efficacy and severe resistance. There is an urgent need to discover antifungal lead compounds with novel chemical scaffold. On the basis of our previously identified tetrahydrocarbazole antifungal leads, the structure-activity relationship was further explored by modifying the scaffold and the side chains. Several targeted compounds showed potent activity against Candida species. Particularly, compound 13i showed better antifungal activity than the lead compound, which can be used as a good starting point for further optimization.
