97389-25-8 Usage
Uses
Used in Pharmaceutical Industry:
3-(4-hydroxyphenyl)-1,3-oxazolidin-2-one is used as a chiral inductor in the synthesis of chiral compounds for its ability to induce chirality, which is crucial in the development of pharmaceuticals that require specific stereochemistry for biological activity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-(4-hydroxyphenyl)-1,3-oxazolidin-2-one is utilized as a building block for the synthesis of biologically active compounds, leveraging its unique structural features to create new molecules with potential therapeutic applications.
Used in Drug Synthesis:
3-(4-hydroxyphenyl)-1,3-oxazolidin-2-one is employed in the synthesis of drugs, where its chiral properties are essential for creating enantiomerically pure compounds that can interact specifically with biological targets, thus enhancing the efficacy and safety of the resulting medications.
Check Digit Verification of cas no
The CAS Registry Mumber 97389-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,8 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97389-25:
(7*9)+(6*7)+(5*3)+(4*8)+(3*9)+(2*2)+(1*5)=188
188 % 10 = 8
So 97389-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO3/c11-8-3-1-7(2-4-8)10-5-6-13-9(10)12/h1-4,11H,5-6H2
97389-25-8Relevant academic research and scientific papers
Studies on Cytotoxicity Associated with Melanin Pigmentation: Attempted Synthesis of N-4-Hydroxyphenylaziridine
Fayadh, J. M.,Swan, G. A.
, p. 222 - 224 (2007/10/02)
In an attempt to synthesise N-4-hydroxyphenylaziridine (II), a derivative of II in which the hydroxyl group is protected has been prepared.However, removal of protective group without concomitant opening of the aziridine ring has not been successful.
