338786-76-8 Usage
Uses
Used in Organic Synthesis:
(+)-N-(3-chloro-2-hydroxypropoxy)phthalimide is utilized as a reagent for the introduction of the phthalimide moiety into other molecules. Its unique structure allows for the creation of a variety of new compounds with potential applications in various fields.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (+)-N-(3-chloro-2-hydroxypropoxy)phthalimide serves as an intermediate in the synthesis of drugs. Its ability to be incorporated into complex molecular structures makes it a valuable component in the development of new medications.
Used in Agrochemical Synthesis:
Similarly, in agrochemicals, (+)-N-(3-chloro-2-hydroxypropoxy)phthalimide is used as an intermediate for the synthesis of various products. Its role in creating effective and targeted agrochemicals contributes to its importance in this sector.
Used in Antifungal Applications:
(+)-N-(3-chloro-2-hydroxypropoxy)phthalimide has been studied for its potential as an antifungal agent. Its ability to combat fungal infections makes it a candidate for use in treatments and preventative measures against fungal diseases.
Used as a Precursor for Anti-Inflammatory and Antitumor Compounds:
Furthermore, (+)-N-(3-chloro-2-hydroxypropoxy)phthalimide has been researched for its potential as a precursor in the synthesis of compounds with anti-inflammatory and antitumor properties. Its role in creating therapeutic agents for these conditions highlights its versatility and potential impact on human health.
Check Digit Verification of cas no
The CAS Registry Mumber 338786-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,7,8 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 338786-76:
(8*3)+(7*3)+(6*8)+(5*7)+(4*8)+(3*6)+(2*7)+(1*6)=198
198 % 10 = 8
So 338786-76-8 is a valid CAS Registry Number.
338786-76-8Relevant academic research and scientific papers
Synthesis and lipase-catalyzed acetylation of N-[(2- alkoxycarbonyl)benzoyl]-4-hydroxyisoxazolidines
Buchalska, Ewa,Plenkiewicz, Jan
, p. 1467 - 1477 (2007/10/03)
Several N-[(2-alkoxycarbonyl)benzoyl]-4- hydroxyisoxazolidines were prepared as the racemic mixtures, and resolved by the lipase-mediated acylation.
Unusual Reaction of N-Hydroxyphthalimido Ethers Leading to Oxygen-Nitrogen Heterocycles
Amlaiky, Nourdine,Leclerc, Gerard,Carpy, Alain
, p. 517 - 523 (2007/10/02)
Treatment of N-phthalimide (1) with alcohols under basic catalysis yields a new 3--5-(hydroxymethyl)-6H-1,4,2-dioxazine (4a) compound, whose structure was determined by X-ray crystallography.Similary, the beha
