54903-55-8 Usage
Uses
Used in Pharmaceutical Development:
AHPTM is utilized as a key compound in the development of pharmaceutical drugs due to its potential for various biological activities. Its unique structure allows for further investigation and potential therapeutic applications, particularly in the areas of anti-inflammatory and antineoplastic treatments.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, AHPTM serves as a subject of research for its potential to contribute to the creation of novel drugs. (4-amino-3-hydroxyphenyl)(thiophen-2-yl)methanone's amino and hydroxy functional groups, along with its thiophen-2-yl and methanone moieties, make it a promising candidate for the exploration of new drug candidates with potential applications in treating various diseases and conditions.
Used in Antineoplastic Applications:
AHPTM is employed as an antineoplastic agent, indicating its potential use in the treatment of cancer. (4-amino-3-hydroxyphenyl)(thiophen-2-yl)methanone's structure and functional groups may contribute to its ability to inhibit or interfere with the growth and spread of cancer cells, making it a valuable asset in the development of cancer therapies.
Used in Anti-inflammatory Applications:
AHPTM also has potential applications in anti-inflammatory treatments. Its biological activities suggest that it may be effective in reducing inflammation, which could be beneficial in the management of various inflammatory conditions and diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 54903-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,0 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54903-55:
(7*5)+(6*4)+(5*9)+(4*0)+(3*3)+(2*5)+(1*5)=128
128 % 10 = 8
So 54903-55-8 is a valid CAS Registry Number.
54903-55-8Relevant academic research and scientific papers
Unequivocal Preparation of 4- and 5-Acyl-2-aminophenols
Aichaoui, Hocine,Lesieur, Isabelle,Henichart, Jean-Pierre
, p. 679 - 680 (2007/10/02)
Unequivocal methods for the specific preparation of 4- or 5-acyl-2-aminophenols are reported. 5-Acyl-2-aminophenols are obtained by ring opening with dilute sodium hydroxide of 2(3H)-benzoxazolinones acylated at position 6. 4-Acyl-2-aminophenols are obtai
6 Acylbenzoxazolinone derivatives. II. Preparation of some transformation products
Bonte,Lesieur,Lespagnol,et al.
, p. 497 - 500 (2007/10/08)
Some transformation products of acylbenzoxazolinones (aminophenols, alcohols, and chalcone derivatives) are described. Preliminary pharmacodynamic study showed analgesic activity.
