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H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride

  CAS No.: 2560614-20-0   Cat No.: BADC-01733 4.5  

H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride, a norbornene-derivatized lysine, can be click-functionalized.

H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride

Structure of 2560614-20-0

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Molecular Formula
C15H25ClN2O4
Molecular Weight
332.82

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IUPAC Name
(2S)-2-amino-6-(2-bicyclo[2.2.1]hept-5-enylmethoxycarbonylamino)hexanoic acid;hydrochloride
Canonical SMILES
C1C2CC(C1C=C2)COC(=O)NCCCCC(C(=O)O)N.Cl
InChI
InChI=1S/C15H24N2O4.ClH/c16-13(14(18)19)3-1-2-6-17-15(20)21-9-12-8-10-4-5-11(12)7-10;/h4-5,10-13H,1-3,6-9,16H2,(H,17,20)(H,18,19);1H/t10?,11?,12?,13-;/m0./s1
InChIKey
ROPKXWIKSNAOMG-HDOKGEMUSA-N

H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride is a specialized chemical compound with diverse applications in bioscience and industry. Here are four key applications of H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride:

Peptide Synthesis: Utilizing H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride as a foundational component in the intricate synthesis of peptides and proteins, researchers can imbue peptide chains with functional groups that facilitate extensive chemical modifications. This capability is essential for crafting therapeutic peptides and deciphering the intricacies of protein-protein interactions.

Drug Delivery Systems: This compound plays a pivotal role in advancing drug delivery technologies, enabling the creation of sophisticated systems for precise drug administration. Through the attachment of therapeutic agents facilitated by functional groups in H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride, targeted and controlled drug release becomes achievable, enhancing drug efficacy while minimizing adverse effects through localized drug delivery strategies.

Bioconjugation: H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride serves as a linchpin in bioconjugation methodologies, acting as a bridge to link biomolecules such as proteins, antibodies, or nucleic acids to various labels or biomolecules. The norbornene group’s presence facilitates efficient and selective conjugation reactions, elevating the stability and functionality of the conjugated products. Widely utilized in diagnostics and therapeutic advancements, this application underscores the compound’s versatility and significance in bioengineering.

Polymer Chemistry: In the realm of polymer chemistry, H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride emerges as a catalyst for innovation in crafting functionalized polymers with tailored properties. The incorporation of polymerizable groups enabled by the norbornene moiety empowers researchers to fashion specialized polymers with unique characteristics, opening avenues for applications in diverse fields such as materials science, coatings, and biomedical engineering. This synergy of chemical design and functionality underscores the compound’s pivotal role in advancing polymer science and engineering efficiencies.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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