1217512-55-4 Usage
Description
(2R)-1-(((9H-Fluoren-9-yl)Methoxy)carbonyl)octahydro-1H-indole-2-carboxylic acid is a complex organic molecule characterized by the presence of a fluorene moiety, an indole group, and a carboxylic acid group. The fluorene moiety is a polycyclic aromatic hydrocarbon, while the indole group is a molecule structure found in many natural organic compounds, including certain amino acids. The carboxylic acid group suggests that this compound could exhibit acidic properties under specific conditions. Additionally, the presence of a methoxy group indicates the potential for methylation in biological or chemical reactions. However, due to the lack of publicly available, peer-reviewed research, the specific applications, toxicity, and role of this compound in biochemistry remain largely unknown.
Uses
Given the limited information available on (2R)-1-(((9H-Fluoren-9-yl)Methoxy)carbonyl)octahydro-1H-indole-2-carboxylic acid, it is challenging to list specific applications. However, based on the presence of various functional groups, some potential uses in different industries can be hypothesized:
Used in Pharmaceutical Industry:
(2R)-1-(((9H-Fluoren-9-yl)Methoxy)carbonyl)octahydro-1H-indole-2-carboxylic acid could be used as a building block or intermediate in the synthesis of pharmaceutical compounds due to its complex structure and the presence of various functional groups.
Used in Chemical Research:
(2R)-1-(((9H-Fluoren-9-yl)Methoxy)carbonyl)octahydro-1H-indole-2-carboxylic acid may serve as a subject of study in chemical research, particularly in the fields of organic synthesis, medicinal chemistry, and biochemistry, to explore its properties, reactivity, and potential applications.
Used in Material Science:
The presence of aromatic rings and functional groups in (2R)-1-(((9H-Fluoren-9-yl)Methoxy)carbonyl)octahydro-1H-indole-2-carboxylic acid may make it a candidate for the development of new materials with specific properties, such as optoelectronic materials or polymers with unique characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 1217512-55-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,5,1 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1217512-55:
(9*1)+(8*2)+(7*1)+(6*7)+(5*5)+(4*1)+(3*2)+(2*5)+(1*5)=124
124 % 10 = 4
So 1217512-55-4 is a valid CAS Registry Number.
1217512-55-4Relevant articles and documents
Exploring hydrophobicity limits of polyproline helix with oligomeric octahydroindole-2-carboxylic acid
Kubyshkin, Vladimir,Budisa, Nediljko
, (2018/03/30)
The polyproline-II helix is the most extended naturally occurring helical structure and is widely present in polar, exposed stretches and “unstructured” denatured regions of polypeptides. Can it be hydrophobic? In this study, we address this question usin
PEPTIDES HAVING BRADYKININ ANTAGONIST ACTION
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, (2008/06/13)
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