14297-59-7 Usage
Chemical class
Terephthalate esters
Organic compound
Yes
Derived from
Terephthalic acid
Contains
Two aniline groups
Common use
Production of polymers (polyesters and polyamides)
Utilized as
Building block for synthesis of various materials
Potential applications
Pharmaceuticals and organic electronics
Reason for potential applications
Unique molecular structure and properties
Check Digit Verification of cas no
The CAS Registry Mumber 14297-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,9 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14297-59:
(7*1)+(6*4)+(5*2)+(4*9)+(3*7)+(2*5)+(1*9)=117
117 % 10 = 7
So 14297-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H24N2O4/c1-3-29-23(27)19-15-22(26-18-13-9-6-10-14-18)20(24(28)30-4-2)16-21(19)25-17-11-7-5-8-12-17/h5-16,25-26H,3-4H2,1-2H3
14297-59-7Relevant articles and documents
Palladium-Catalyzed Approach to Malasseziazole A and First Total Synthesis of Malasseziazole C
Kober, Ute,Kn?lker, Hans-Joachim
, p. 1549 - 1552 (2015)
We describe a convergent route to 5,11-dihydroindolo[3,2-b]carbazoles using a twofold oxidative cyclization as key step. The method has been applied to the synthesis of a precursor for malasseziazole A and to the first total synthesis of malasseziazole C.
Syntheses of 6,12-disubstituted 5,11-dihydroindolo[3,2-b]carbazoles, including 5,11-dihydroindolo[3,2-b]carbazole-6,12-dicarbaldehyde, an extremely efficient ligand for the TCDD (Ah) receptor
Tholander, Joakim,Bergman, Jan
, p. 12577 - 12594 (2007/10/03)
Symmetrically and unsymmetrically 6,12-disubstituted 5,11- dihydroindolo[3,2-b]carbazoles have been synthesized via a range of methods: a)double Fischer indolization of the bis-phenylhydrazone of 2,5-dimethyl-1,4- cyclohexanedione, b) condensation of indo
