4508-93-4 Usage
Chemical structure
A complex organic compound with a long chemical name.
Derivative
A derivative of naphthalene.
Functional groups
Contains both an amino group and a hydroxyl group.
Synthesis
Can be synthesized for research and industrial applications.
Potential uses
May have potential uses in the pharmaceutical industry due to its complex structure and potential biological activity.
Further research
Further research is needed to understand its properties and potential applications.
Please note that this list is based on the limited information provided in the material and may not be exhaustive. Additional research and analysis would be required to provide a more comprehensive understanding of the compound's properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4508-93-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,0 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4508-93:
(6*4)+(5*5)+(4*0)+(3*8)+(2*9)+(1*3)=94
94 % 10 = 4
So 4508-93-4 is a valid CAS Registry Number.
4508-93-4Relevant academic research and scientific papers
Synthesis of dioxazaborocines from N-substituted-bis(2-hydroxyaryl)aminomethylamines
Woodgate, Paul D.,Horner, Gillian M.,Maynard, N. Paul,Rickard, Clifton E.F.
, p. 180 - 193 (2007/10/03)
The preparation of a number of tripodal amines from aminoalkylation of 1,3-benzoxazines by phenols is presented. A series of ligands prepared in this manner were successfully coordinated to boron, giving dioxazaborocines. X-ray crystal structures of two analogues are reported. These compounds are capable of releasing borate ions and are therefore potentially biologically active.
Synthesis of Dihydrobenzofurans from Phenolic Mannich Bases and their Quaternized Derivatives
Blade-Font, Artur,Rocabayera, Teodoro de Mas
, p. 841 - 848 (2007/10/02)
Reaction of dimethylsulphoxonium methylide with quaternized derivatives of phenolic Mannich bases, and in certain cases with the bases themselves, constitutes a useful synthesis of dihydrobenzofurans.On the other hand treatment of those same quaternized derivatives with diazomethane may be a useful alternative procedure for the preparation of coumarans with base-sensitive groups.