5555-22-6 Usage
Uses
Used in Pharmaceutical Synthesis:
N-BENZYL ASPARTIC ACID is used as a building block for the synthesis of various pharmaceuticals and organic compounds, leveraging its unique chemical structure to create novel therapeutic agents.
Used in Enzyme Inhibition:
N-BENZYL ASPARTIC ACID is used as an inhibitor of the enzyme acetylcholinesterase, which is implicated in Alzheimer's disease, for its potential role in managing or treating this condition.
Used in Drug Delivery Systems Development:
N-BENZYL ASPARTIC ACID is used in the development of new drug delivery systems and materials, due to its unique properties that can enhance the efficacy and targeted delivery of therapeutic agents.
Used in Medicinal Chemistry:
N-BENZYL ASPARTIC ACID is used as a research tool in medicinal chemistry to explore its potential biological activities and to understand its interactions with biological targets, contributing to the advancement of drug discovery.
Used in Materials Science:
N-BENZYL ASPARTIC ACID is used in the field of materials science to develop new materials with specific properties, taking advantage of its chemical structure to create innovative applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5555-22-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5555-22:
(6*5)+(5*5)+(4*5)+(3*5)+(2*2)+(1*2)=96
96 % 10 = 6
So 5555-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4/c13-10(14)6-9(11(15)16)12-7-8-4-2-1-3-5-8/h1-5,9,12H,6-7H2,(H,13,14)(H,15,16)/t9-/m0/s1
5555-22-6Relevant academic research and scientific papers
Direct synthesis of N-substituted, functionalized aspartic acids using alkali maleates and amines
Piispanen, Peter S.,Pihko, Petri M.
, p. 2751 - 2755 (2007/10/03)
A practical and general one-pot synthesis of mono-N-substituted, functionalized aspartic acids has been developed. The N-substituted aspartic acids are formed directly from alkali maleates and primary amines in hot DMSO. Products from several different primary amines can be prepared chemoselectively in moderate to good yields.
