102421-85-2 Usage
Fused tricyclic structure
The compound has a complex structure consisting of three fused rings, which are benzene, benzopyran, and acridine rings.
Composition
It is composed of benzene, benzopyran, and acridine rings, which are all aromatic in nature.
Hydroxyl groups
The compound contains two hydroxyl (-OH) groups, which can participate in hydrogen bonding and other interactions.
Polyaromatic hydrocarbon
It is a type of polyaromatic hydrocarbon, which means it has multiple aromatic rings in its structure.
Potential biological activities
Due to its intricate structure, 1a,2,3,13c-tetrahydrobenzo[h][1]benzoxireno[2,3-a]acridine-2,3-diol may have potential biological activities, making it a subject of interest for research in medicinal chemistry.
Photophysical properties
The presence of multiple aromatic rings suggests that the compound may exhibit interesting photophysical properties, such as absorption and emission of light.
Photochemical properties
The compound may also have interesting photochemical properties, which could be relevant for research in organic chemistry and the development of new chemical reactions.
Research interest
Due to its unique structure and potential properties, 1a,2,3,13c-tetrahydrobenzo[h][1]benzoxireno[2,3-a]acridine-2,3-diol is a subject of interest for research in the fields of organic chemistry and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 102421-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,2 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102421-85:
(8*1)+(7*0)+(6*2)+(5*4)+(4*2)+(3*1)+(2*8)+(1*5)=72
72 % 10 = 2
So 102421-85-2 is a valid CAS Registry Number.
102421-85-2Relevant articles and documents
Synthesis of Dihydrodiols and Diol Epoxides of Dibenzacridine
Kumar, Subodh,Agarwal, Nand L.
, p. 2445 - 2449 (2007/10/02)
trans-1,2-Dihydroxy-1,2-dihydrodibenzacridine (5), trans-3,4-dihydroxy-3,4-dihydrodibenzacridine (6), trans-8,9-dihydroxy-8,9-dihydrodibenzacridine (7), 3α,4β-dihydroxy-1α,2α-epoxy-1,2,3,4-tetrahydrodibenzacridine (9), and 3α,4β-dihydroxy-1β,2β-epoxy-1,2,3,4-tetrahydrodibenzacridine (10), which are potentially proximate and ultimate carcinogens of dibenzacridine (1), are synthesized from a common intermediate 8,9,10,11-tetrahydrodibenzacridine (13).The Birch reduction of 13 produced an intermediate which has been used in preparing 5 and 6.However, the bromination of 13 followed by dehydrobromination resulted in a mixture of isomeric alkenes which was successfully converted to 7. 1H NMR, UV, and mass spectra of dibenzacridine derivatives are reported.
