94718-66-8 Usage
Derivative of azacarbazole
A derivative of the heterocyclic compound azacarbazole This compound is based on the azacarbazole structure, which contains a five-membered nitrogen-containing ring fused to a six-membered carbon ring.
Carboxylic acid
Contains a carboxyl group (-COOH) 1-azacarbazole-6-carboxylic acid has a carboxyl functional group, which gives it acidic properties.
Acidic nature
The presence of the carboxyl group (-COOH) makes the compound acidic in nature.
Potential applications in organic synthesis
Due to its unique structural and chemical properties, 1-azacarbazole-6-carboxylic acid can be used as an intermediate or building block in organic synthesis.
Potential applications in medicinal chemistry
The compound may have potential biological activities, making it of interest for pharmacological research and the development of new drugs.
Potential applications in materials science
1-azacarbazole-6-carboxylic acid may be used in the development of new materials with unique properties due to its structural and chemical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 94718-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,7,1 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94718-66:
(7*9)+(6*4)+(5*7)+(4*1)+(3*8)+(2*6)+(1*6)=168
168 % 10 = 8
So 94718-66-8 is a valid CAS Registry Number.
94718-66-8Relevant articles and documents
Synthesis of 6-substituted pyrido[2,3-b]indoles by electrophilic substitution
Schneider, Cédric,Gueyrard, David,Popowycz, Florence,Joseph, Beno?t,Goekjian, Peter G.
, p. 2237 - 2241 (2008/02/10)
Regioselective electrophilic aromatic substitutions, acylation, bromination, and formylation, of unprotected pyrido[2,3-b]indole (α-carbolines) at the C-6 position are described. Alternative conditions for the nitration were investigated, which led to the unexpected appearance of the minor C-8 isomer. Georg Thieme Verlag Stuttgart.
