173522-95-7 Usage
Uses
Used in Pharmaceutical Industry:
3,4-Dichloro-L-Phenylalanine Methyl ester is used as a building block for the synthesis of pharmaceutical compounds and drug candidates. Its unique structure and functional groups make it a versatile component in the development of new medications.
Used in Research Applications:
3,4-Dichloro-L-Phenylalanine Methyl ester is used as a research tool to study its potential biological activity. It has been investigated for its possible anticancer properties, providing insights into the development of new cancer therapies.
Used in Anticancer Applications:
3,4-Dichloro-L-Phenylalanine Methyl ester is used as a potential anticancer agent. Its biological activity has been studied, and it may contribute to the development of new cancer treatments by targeting specific pathways or mechanisms involved in cancer progression.
Overall, 3,4-Dichloro-L-Phenylalanine Methyl ester is a multifaceted chemical compound with significant applications in the pharmaceutical and research sectors, particularly in the development of new drugs and therapies for various diseases, including cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 173522-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,5,2 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 173522-95:
(8*1)+(7*7)+(6*3)+(5*5)+(4*2)+(3*2)+(2*9)+(1*5)=137
137 % 10 = 7
So 173522-95-7 is a valid CAS Registry Number.
173522-95-7Relevant academic research and scientific papers
Rhodium-Catalyzed Enantioselective Synthesis of Oxazinones via an Asymmetric Ring Opening-Lactonization Cascade of Oxabicyclic Alkenes
Yen, Andy,Pham, Anh Hoang,Larin, Egor M.,Lautens, Mark
supporting information, p. 7549 - 7553 (2019/10/02)
The rhodium-catalyzed asymmetric ring opening reaction of oxabicyclic alkenes is shown to be an efficient method for synthesizing chiral heterocycles. We demonstrate that the pairwise combination of chiral catalyst with chiral amino-acid-derived pronucleophiles results in a stereodivergent synthesis of diastereomeric hydroxyesters. A favorable conformational preference induces the subsequent lactonization of one diastereomer leading to the highly enantioselective synthesis of oxazinones.
SULFONAMIDE COMPOUNDS
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Page/Page column 18, (2010/10/20)
Certain sulfonamide compounds are dual CCK1/CCK2 inhibitors useful in the treatment of CCK1/CCK2 mediated diseases.
