55362-76-0 Usage
Description
TERT-BUTOXYCARBONYLAMINO-(4-METHOXY-PHENYL)-ACETIC ACID, with the molecular formula C15H21NO5, is a chemical compound that plays a significant role in medicinal chemistry. It is recognized for its potential as a precursor in the synthesis of pharmaceutical drugs, offering a foundation for the development of novel medications targeting various medical conditions. Its capacity to act as an enzyme inhibitor and its demonstrated efficacy in treating inflammation, pain, and neurodegenerative diseases make it a promising candidate for therapeutic innovation.
Uses
Used in Pharmaceutical Industry:
TERT-BUTOXYCARBONYLAMINO-(4-METHOXY-PHENYL)-ACETIC ACID is used as a chemical precursor for the synthesis of pharmaceutical drugs, leveraging its structural properties to create new medications for a range of medical conditions.
Used in Enzyme Inhibition:
In the field of medicinal chemistry, TERT-BUTOXYCARBONYLAMINO-(4-METHOXY-PHENYL)-ACETIC ACID is utilized as an enzyme inhibitor, contributing to the development of treatments that can modulate biological processes at the molecular level.
Used in Inflammation Treatment:
TERT-BUTOXYCARBONYLAMINO-(4-METHOXY-PHENYL)-ACETIC ACID is employed as an anti-inflammatory agent, potentially mitigating the effects of inflammation in various conditions.
Used in Pain Management:
This chemical compound is used in the development of pain management medications, offering a new avenue for treating acute and chronic pain conditions.
Used in Neurodegenerative Disease Treatment:
TERT-BUTOXYCARBONYLAMINO-(4-METHOXY-PHENYL)-ACETIC ACID is used in the research and development of treatments for neurodegenerative diseases, with the aim of slowing disease progression or improving patient outcomes.
Overall, TERT-BUTOXYCARBONYLAMINO-(4-METHOXY-PHENYL)-ACETIC ACID is a versatile and valuable tool in the pharmaceutical industry, with applications that span across multiple therapeutic areas, making it instrumental in the advancement of new therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 55362-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55362-76:
(7*5)+(6*5)+(5*3)+(4*6)+(3*2)+(2*7)+(1*6)=130
130 % 10 = 0
So 55362-76-0 is a valid CAS Registry Number.
55362-76-0Relevant articles and documents
Synthesis ofN-Boc-α-amino Acids from Carbon Dioxide by Electrochemical Carboxylation ofN-Boc-α-aminosulfones
Senboku, Hisanori,Minemura, Yoshihito,Suzuki, Yuto,Matsuno, Hidetoshi,Takakuwa, Mayu
, p. 16077 - 16083 (2021/10/12)
Electrochemical reduction ofN-Boc-α-aminosulfones in DMF using an undivided cell equipped with a Pt plate cathode and an Mg rod anode under atmospheric pressure of bubbling carbon dioxide through the solution under constant current conditions resulted in a reductive C-S bond cleavage with elimination of benzenesulfinate ion generating the corresponding anion species followed by fixation of carbon dioxide to give the correspondingN-Boc-α-amino acids in moderate to good yields.
GLYCINE DERIVATIVES AND MEDICINAL COMPOSITIONS THEREOF
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Page/Page column 27, (2012/06/16)
Alkaloid aminoester derivatives according to formula (I) and (VI) act as muscarinic receptor antagonists.
2-ARYL GLYCINAMIDE DERIVATIVES
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Page/Page column 29, (2010/01/29)
The disclosure provides compounds of Formula I, including pharmaceutically acceptable salts, their pharmaceutical compositions, and their uses in inhibiting β-amyloid peptide ( β-AP) production.
