36747-66-7 Usage
Uses
Used in Pharmaceutical Synthesis:
2-(CBZ-AMINO)-2-(4'-HYDROXYPHENYL)ACETIC ACID serves as a key intermediate in the development of various pharmaceutical compounds. Its chemical structure allows for the creation of novel drugs with potential therapeutic benefits in treating a range of diseases and conditions.
Used in Drug Delivery Systems:
In the field of drug delivery, 2-(CBZ-AMINO)-2-(4'-HYDROXYPHENYL)ACETIC ACID is utilized for its potential role in enhancing the efficacy and targeted delivery of pharmaceutical agents. Its chemical properties make it suitable for the design of controlled release formulations, improving the pharmacokinetics and therapeutic outcomes of associated drugs.
Used in Research and Development:
2-(CBZ-AMINO)-2-(4'-HYDROXYPHENYL)ACETIC ACID is also employed in research settings to explore its potential applications in medicine. Ongoing studies aim to uncover its therapeutic potential, particularly in the treatment of various diseases and conditions, and to innovate new drug delivery approaches leveraging its chemical attributes.
Used in Chemical Modification of Bioactive Molecules:
2-(CBZ-AMINO)-2-(4'-HYDROXYPHENYL)ACETIC ACID is applied in the chemical modification of bioactive molecules to enhance their stability, bioavailability, and overall effectiveness. This application is crucial in optimizing the performance of drugs and other bioactive agents in medical and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 36747-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,4 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36747-66:
(7*3)+(6*6)+(5*7)+(4*4)+(3*7)+(2*6)+(1*6)=147
147 % 10 = 7
So 36747-66-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H15NO5/c18-13-8-6-12(7-9-13)14(15(19)20)17-16(21)22-10-11-4-2-1-3-5-11/h1-9,14,18H,10H2,(H,17,21)(H,19,20)
36747-66-7Relevant academic research and scientific papers
Process for preparing substituted glycines
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, (2008/06/13)
A new process is disclosed for the preparation of N-acyl-α-aromatic and N-acyl-α-heteroaromatic glycines by reaction of an α-ester or ether of an N-acylglycine ester or acid with an aromatic or heteroaromatic compound. Also disclosed are new intermediates for preparing N-acyl-α-aromatic and N-acyl-α-heteroaromatic glycines.
