62396-48-9 Usage
Description
Boc-D-Aspartic acid, also known as N-Boc-D-aspartic acid, is an N-Boc-protected form of D-Aspartic acid (A790020). D-Aspartic acid is the unnatural isomer of L-Aspartic acid (A790024) and is naturally found in human ovarian follicular fluid, where it is believed to be associated with oocyte quality. Additionally, it is present in the white matter of human brains, particularly in myelin proteins. Boc-D-Aspartic acid is a white powder and is utilized in various applications across different industries due to its unique properties.
Uses
Used in Pharmaceutical Industry:
Boc-D-Aspartic acid is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its role in the pharmaceutical industry is crucial, as it aids in the development of drugs targeting specific conditions related to the presence and function of D-Aspartic acid in the human body.
Used in Research and Development:
In the field of research and development, Boc-D-Aspartic acid is used as a key component in the study of the properties and functions of D-Aspartic acid. It helps researchers understand the role of D-Aspartic acid in various biological processes and its potential implications in human health and disease.
Used in Biochemical Applications:
Boc-D-Aspartic acid is used as a building block in the synthesis of peptides and other biomolecules for [application reason]. Its unique properties make it a valuable asset in the development of novel bioactive compounds with potential applications in various industries, including pharmaceuticals, agriculture, and materials science.
Used in Diagnostics:
Boc-D-Aspartic acid is used as a diagnostic marker for [application reason]. Its presence in human ovarian follicular fluid and the white matter of human brains makes it a potential indicator for various conditions related to fertility and neurological disorders. By measuring the levels of Boc-D-Aspartic acid, medical professionals can gain insights into the health of a patient's reproductive and neurological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 62396-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,9 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62396-48:
(7*6)+(6*2)+(5*3)+(4*9)+(3*6)+(2*4)+(1*8)=139
139 % 10 = 9
So 62396-48-9 is a valid CAS Registry Number.
62396-48-9Relevant articles and documents
Morphological control of self-assembled multivalent (SAMul) heparin binding in highly competitive media
Rodrigo, Ana C.,Bromfield, Stephen M.,Laurini, Erik,Posocco, Paola,Pricl, Sabrina,Smith, David K.
supporting information, p. 6335 - 6338 (2017/07/11)
Tuning molecular structures of self-assembling multivalent (SAMul) dendritic cationic lipopeptides controls the self-assembled morphology. In buffer, spherical micelles formed by higher generation systems bind polyanionic heparin better than worm-like micelles formed by lower generation systems. In human serum, the binding of spherical micelles to heparin is adversely affected, while worm-like micelles maintain their relative binding ability.
HYDROLYSE ENANTIOSELECTIVE D'ESTERS D'AMINOACIDE CATALYSEE PAR L'IMIDAZOLE DANS DES MICELLES INVERSES CHIRALES.1300
Andriamanampisoa, R.,Boyer, B.,Lamity, G.,Roque, J. P.
, p. 77 - 84 (2007/10/02)
This paper reports the study of the imidazole catalyzed hydrolysis of enantiomeric pairs of three aminoacid esters in reversed micelles prepared from water, heptane and a combination of both racemic or chiral surfactants and of both racemic or chiral (S)2-octanol as cosurfactants.The enantioselectivity observed is important in the combination of chiral surfactant with racemic cosurfactant, and small in the combination of racemic surfactant with chiral cosurfactant, when ω = 20 (ω = / ).This enantioselectivity is also affected by the nature of the cosurfactant, the size of micelles and the nature of the substrate.The results prove that the reaction occurs effectively in a chiral microenvironment, the micelle membrane, and indicate that the cosurfactant is actually present in this membrane.