4852-91-9 Usage
Uses
Used in Pharmaceutical Applications:
2-amino-5-(octyloxy)-5-oxopentanoic acid (non-preferred name) can be utilized as a building block or a modifying agent in the development of new pharmaceutical compounds. Its unique structure may allow for the creation of drugs with specific targeting or delivery properties, potentially enhancing the efficacy and selectivity of therapeutic agents.
Used in Polymer Science:
In the field of polymer science, 2-amino-5-(octyloxy)-5-oxopentanoic acid (non-preferred name) may serve as a monomer or a comonomer in the synthesis of novel polymers with tailored properties. The incorporation of 2-amino-5-(octyloxy)-5-oxopentanoic acid (non-preferred name) into polymer chains could lead to materials with improved characteristics, such as enhanced stability, solubility, or biocompatibility.
Used in Materials Science:
2-amino-5-(octyloxy)-5-oxopentanoic acid (non-preferred name) may also find applications in materials science, where its unique structure could be employed to create new materials with specific properties. These materials could have potential uses in various industries, such as coatings, adhesives, or even in the development of new energy storage or conversion technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 4852-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4852-91:
(6*4)+(5*8)+(4*5)+(3*2)+(2*9)+(1*1)=109
109 % 10 = 9
So 4852-91-9 is a valid CAS Registry Number.
4852-91-9Relevant academic research and scientific papers
The effect of alkyl side groups on the secondary structure and crystallization of poly(ethylene glycol)-block-polypeptide copolymers
Ren, Kaixuan,Cheng, Yilong,He, Chaoliang,Xiao, Chunsheng,Li, Gao,Chen, Xuesi
, p. 2466 - 2472 (2013/06/05)
The solid state and melt nanoscale structures of a series of poly(ethylene glycol)-block-poly(γ-alkyl-l-glutamate)s (PEG-b-PALG) copolymers bearing different alkyl side groups, i.e., n-butyl, n-hexyl, n-octyl, and n-dodecyl, have been investigated in the present work. An interesting effect of alkyl side groups on the secondary conformation of polypeptide block, crystallization of PEG segments and morphology of the copolymers was observed. With increasing the length of alkyl side groups or raising the temperature, the predominant secondary structure gradually changed from α-helix to β-sheet conformation. Differential scanning calorimetry, wide-angle X-ray diffraction analysis and polarized optical microscopy indicated that the crystallization and morphology of PEG segments were markedly restricted by the polypeptide block. Therefore, the alkyl side groups not only exhibited significant influence on the conformation of polypeptide block, but also affected the crystallization of PEG segments. The secondary structure, crystallization and spherulite morphology of these synthetic biomaterials, which were significantly influenced by alkyl side groups, may play an important role in their physicochemical properties, such as self-assembly, as well as in some biomedical applications.
