3814-46-8 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
2-Aminocycloheptanecarboxylic acid is utilized as a building block for the design and synthesis of novel bioactive compounds. Its unique cyclic structure and amino group provide opportunities for the development of new pharmaceutical agents with distinct properties and therapeutic applications.
Used in Peptide and Protein Synthesis:
As a cyclic amino acid, 2-Aminocycloheptanecarboxylic acid is used in the synthesis of peptides and proteins with specific structural and functional characteristics. Its incorporation into peptide sequences can lead to the creation of new bioactive molecules with potential applications in medicine and biotechnology.
Used in Chemical and Biochemical Product Synthesis:
2-Aminocycloheptanecarboxylic acid serves as a starting material for the synthesis of a wide range of chemical and biochemical products. Its versatile structure allows for various chemical modifications and reactions, enabling the production of diverse compounds for use in different industries, such as pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 3814-46-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,1 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3814-46:
(6*3)+(5*8)+(4*1)+(3*4)+(2*4)+(1*6)=88
88 % 10 = 8
So 3814-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO2/c9-7-5-3-1-2-4-6(7)8(10)11/h6-7H,1-5,9H2,(H,10,11)
3814-46-8Relevant academic research and scientific papers
PEPTIDES AND PEPTIDOMIMETIC COMPOUNDS, THE MANUFACTURING THEREOF AS WELL AS THEIR USE FOR PREPARING A THERAPEUTICALLY AND/OR PREVENTIVELY ACTIVE PHARMACEUTICAL COMPOSITION
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, (2010/04/25)
Peptides, peptidomimetics and derivatives thereof of the general formula I: H2N-GHRPX1-β-X4X5X6X7X8X9X10-X11 (I), in which X1-X10 denote one of the 20 genetically coded amino acids, wherein X8, X9 and X10 may also denote a single chemical bond;X11 denotes OR1 in which R1 equals hydrogen or (C1-C10) alkyl NR2R3 with R2 and R3 are equal or different and denote hydrogen, (C1-C10) alkyl, or a residue —W-PEG5-60K, in which the PEG residue is attached via a suitable spacer W to the N-atom, ora residue NH—Y-Z-PEG5-60K, in whichY denotes a chemical bond or a genetically coded amino acids from the group S, C, K or R andZ denotes a spacer, via which a polyethylene glycol (PEG)-residue can be attached, and their physiologically acceptable salts, andβ denotes an amino acid, or a peptidomimetic element, which induces a bend or turn in the peptide backbone.
