18073-15-9 Usage
General Description
6-Methoxy-1,4-dimethyl-9H-carbazole-3-carbaldehyde is a chemical compound with the molecular formula C16H15NO2. It is a carbazole derivative with a 6-methoxy and 1,4-dimethyl substitution pattern and an aldehyde functional group at the 3-position. 6-Methoxy-1,4-dimethyl-9H-carbazole-3-carbaldehyde is often used as a intermediate for the synthesis of various organic compounds. It has been studied for its potential applications in organic electronics, such as in the development of organic light-emitting diodes (OLEDs) and organic semiconductors. Additionally, it may also exhibit biological activity and has been investigated in the context of medicinal chemistry. Overall, 6-Methoxy-1,4-dimethyl-9H-carbazole-3-carbaldehyde is a versatile and potentially useful chemical compound with a range of possible applications in both industrial and research settings.
Check Digit Verification of cas no
The CAS Registry Mumber 18073-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,7 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18073-15:
(7*1)+(6*8)+(5*0)+(4*7)+(3*3)+(2*1)+(1*5)=99
99 % 10 = 9
So 18073-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H15NO2/c1-9-6-11(8-18)10(2)15-13-7-12(19-3)4-5-14(13)17-16(9)15/h4-8,17H,1-3H3
18073-15-9Relevant articles and documents
Design, synthesis, DNA binding studies and evaluation of anticancer potential of novel substituted biscarbazole derivatives against human glioma U87 MG cell line
Kumar, Nitin,Lal, Neetika,Nemaysh, Vishal,Luthra, Pratibha Mehta
, (2020/06/04)
In this research paper, we report the design and synthesis of novel substituted biscarbazole derivatives which were characterized by 1H and 13C NMR, high resolution mass spectroscopy (HRMS). The SAR study of the compounds is reported
Modifications to the Vilsmeier-Haack formylation of 1,4-dimethylcarbazole and its application to the synthesis of ellipticines
Deane, Fiona M.,Miller, Charlotte M.,Maguire, Anita R.,McCarthy, Florence O.
experimental part, p. 814 - 823 (2011/10/04)
Figure represented. An improved method for the preparation of 3-formyl-1,4-dimethylcarbazole, a key intermediate in the synthesis of ellipticine, is presented. Conditions of the Vilsmeier-Haack reaction have been modified to facilitate the production of 3-formyl-1,4-dimethylcarbazole as a major product leading to an overall improvement in yield of ellipticine from 3% to 14%. This approach was also applied to the synthesis of 6-methylellipticine and 9-methoxyellipticine.
Synthesis of (±) 9-methoxy-4-hydroxy-1,2,3,4-tetrahydroellipticine
Martin-Onraet,Gansser,Plat,et al.
, p. 745 - 754 (2007/10/02)
-