90655-98-4 Usage
Molecular structure
Naphthoindole backbone with a benzoyl, chloro, and phenyl group attached.
Molecular weight
419.85 g/mol
Potential applications
Medicinal chemistry and drug development.
Biological activity
May exhibit biological activity due to its structural features.
Synthesis
Could be used as a building block for the synthesis of novel pharmaceutical compounds.
Pharmacological properties
Potential pharmacological properties need to be studied and tested.
Further research
Additional research and testing required to understand the potential uses and effects of this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 90655-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,5 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90655-98:
(7*9)+(6*0)+(5*6)+(4*5)+(3*5)+(2*9)+(1*8)=154
154 % 10 = 4
So 90655-98-4 is a valid CAS Registry Number.
90655-98-4Relevant articles and documents
REACTION OF BORATE COMPLEXES OF 1,4-DIAMINO- AND 1-AMINO-4-HYDROXYANTHRAQUINONES WITH THE ANIONS OF CH ACIDS
Gorelik, M. V.,Mishina, E. V.
, p. 1892 - 1899 (2007/10/02)
The reaction of the diboroacetates of 1,4-diamino- and 1-amino-4-hydroxyanthraquinones with CH acids in an aprotic polar solvent in the presence of a base leads to the angular 5-amino- and 5-hydroxynaphtoindole-6,11-diones respectively.In the reaction of the diboroacetate of 2,3-dichloro-1,4-diaminoanthraquinone with dibenzoylmethane the main reaction product is the linear 4,11-diaminoanthrafuran-5,10-dione.
