135605-66-2 Usage
Uses
Used in Pharmaceutical Industry:
(S)-3-(4-Hydroxyphenyl)-5-(methoxymethyl)-2-oxazolidinone is used as a potential active pharmaceutical ingredient for the development of new drugs due to its demonstrated anti-inflammatory and analgesic properties. It has shown promise in preclinical studies for the treatment of various medical conditions that require these therapeutic effects.
Used in Antibiotic Development:
In the field of antibiotics, (S)-3-(4-Hydroxyphenyl)-5-(methoxymethyl)-2-oxazolidinone is used as a candidate for new antimicrobial agents. Its antimicrobial activities suggest that it could be a valuable component in the development of novel antibiotics to combat resistant bacterial strains.
Used in Antifungal Medications:
Similarly, in the realm of antifungal medications, (S)-3-(4-Hydroxyphenyl)-5-(methoxymethyl)-2-oxazolidinone is used as a potential antifungal agent. Its antifungal activities indicate that it could contribute to the creation of new medications to treat fungal infections, addressing the need for new treatments in the face of increasing antifungal resistance.
Overall, the compound's multifaceted biological activities and potential applications across different areas of medicine underscore its importance in the pharmaceutical industry, warranting further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 135605-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,0 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135605-66:
(8*1)+(7*3)+(6*5)+(5*6)+(4*0)+(3*5)+(2*6)+(1*6)=122
122 % 10 = 2
So 135605-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4/c1-15-7-10-6-12(11(14)16-10)8-2-4-9(13)5-3-8/h2-5,10,13H,6-7H2,1H3/t10-/m0/s1
135605-66-2Relevant academic research and scientific papers
Practical synthesis of 4,4,4-trifluorocrotonaldehyde: A versatile precursor for the enantioselective formation of trifluoromethylated stereogenic centers via organocatalytic 1,4-additions
Shibatomi, Kazutaka,Narayama, Akira,Abe, Yoshiyuki,Iwasa, Seiji
supporting information; experimental part, p. 7380 - 7382 (2012/10/08)
The practical synthesis of 4,4,4-trifluorocrotonaldehyde (1) and its application to enantioselective 1,4-additions are described. The organocatalytic 1,4-addition of 1 with several nucleophiles such as heteroaromatics, alkylthiols and aldoximes afforded t
