72238-02-9 Usage
Description
N,N-diethyl-N'-(9-methoxy-5,11-dimethyl-6H-pyrido[4,3-b]carbazol-1-yl)propane-1,3-diamine is a complex organic chemical compound that is a derivative of propane-1,3-diamine. It features additional diethyl and 9-methoxy-5,11-dimethyl-6H-pyrido[4,3-b]carbazol-1-yl groups, which may confer unique pharmacological or biological properties to the molecule. Further research and testing are required to explore its potential applications and effects.
Uses
As the provided materials do not specify the uses of N,N-diethyl-N'-(9-methoxy-5,11-dimethyl-6H-pyrido[4,3-b]carbazol-1-yl)propane-1,3-diamine, it is not possible to list its applications based on the given information. However, given its structural complexity and the presence of various functional groups, it may have potential applications in various industries such as pharmaceuticals, agrochemicals, or materials science. Further research would be needed to determine its specific uses and benefits in these or other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 72238-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,3 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72238-02:
(7*7)+(6*2)+(5*2)+(4*3)+(3*8)+(2*0)+(1*2)=109
109 % 10 = 9
So 72238-02-9 is a valid CAS Registry Number.
InChI:InChI=1/C25H32N4O/c1-6-29(7-2)14-8-12-26-25-23-17(4)22-20-15-18(30-5)9-10-21(20)28-24(22)16(3)19(23)11-13-27-25/h9-11,13,15,28H,6-8,12,14H2,1-5H3,(H,26,27)
72238-02-9Relevant articles and documents
Industrial synthesis in mass production. Ellipticine. II. The elaboration of a new approach to GH-pyrido[4,3:b]carbazoles and analogs. B. The recovery of tetracyclic structures
Dormoy,Heymes
, p. 2915 - 2938 (2007/10/02)
Total synthesis of modified ellipticines 1c and 1f is described from 2-chloronicotinic acid and respectively 5-methoxy-indole and 5-azaindole in 11 to 13 steps with overall yields of 11% and 18%. With respect to the numerous synthesis described in the literature, the originality of this approach resides above all in the formation of ring C in basic medium, such conditions being dictated by the presence of the pyridine A ring in the case of 1f. Both synthesis have been extrapolated to produce several kilograms of final product. The second part deals with the elaboration of tetracyclic structures from precursors.