Cas no 275385-03-0 (N-Boc-N-bis(PEG1-OH))

N-Boc-N-bis(PEG1-OH) is a bifunctional polyethylene glycol (PEG) derivative featuring a tert-butoxycarbonyl (Boc) protecting group and dual hydroxyl-terminated PEG arms. This compound is particularly useful in organic synthesis and bioconjugation, offering controlled reactivity due to the Boc group's orthogonality with other functional groups. The dual hydroxyl termini enable further functionalization, facilitating linker formation or polymer modification. Its PEG spacer enhances solubility and reduces steric hindrance, making it suitable for applications in drug delivery, peptide synthesis, and material science. The Boc group allows selective deprotection under mild acidic conditions, ensuring compatibility with sensitive substrates. This reagent is valued for its versatility in constructing complex molecular architectures.
N-Boc-N-bis(PEG1-OH) structure
N-Boc-N-bis(PEG1-OH) structure
Product Name:N-Boc-N-bis(PEG1-OH)
CAS No:275385-03-0
MF:C13H27NO6
MW:293.356584787369
CID:3045641
PubChem ID:85773346
Update Time:2025-06-08

N-Boc-N-bis(PEG1-OH) Chemical and Physical Properties

Names and Identifiers

    • N-Boc-N-bis(PEG1-OH)
    • N-Boc-N-bis(PEG2-OH)
    • tert-butyl bis(2-(2-hydroxyethoxy)ethyl)carbamate
    • tert-butyl N,N-bis[2-(2-hydroxyethoxy)ethyl]carbamate
    • 275385-03-0
    • HY-117079
    • BP-23603
    • EN300-7374294
    • DA-56038
    • SCHEMBL23296185
    • CS-0063666
    • C70845
    • AKOS040742222
    • Inchi: 1S/C13H27NO6/c1-13(2,3)20-12(17)14(4-8-18-10-6-15)5-9-19-11-7-16/h15-16H,4-11H2,1-3H3
    • InChI Key: QKKAOQUTADWQAZ-UHFFFAOYSA-N
    • SMILES: O(C(N(CCOCCO)CCOCCO)=O)C(C)(C)C

Computed Properties

  • Exact Mass: 293.183838g/mol
  • Monoisotopic Mass: 293.183838g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 12
  • Complexity: 242
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.6
  • Topological Polar Surface Area: 88.5
  • Molecular Weight: 293.36g/mol

N-Boc-N-bis(PEG1-OH) Security Information

  • Signal Word:Warning
  • Storage Condition:Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

N-Boc-N-bis(PEG1-OH) Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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Additional information on N-Boc-N-bis(PEG1-OH)

Recent Advances in the Application of 275385-03-0 and N-Boc-N-bis(PEG1-OH) in Chemical Biology and Pharmaceutical Research

The compound with CAS number 275385-03-0 and the product N-Boc-N-bis(PEG1-OH) have recently garnered significant attention in the field of chemical biology and pharmaceutical research. These molecules are pivotal in the development of novel therapeutic agents and drug delivery systems. This research brief aims to synthesize the latest findings related to these compounds, highlighting their applications, mechanisms, and potential impact on the industry.

275385-03-0, a chemically distinct entity, has been investigated for its role in modulating biological pathways. Recent studies have elucidated its potential as a scaffold for designing inhibitors targeting specific enzymes involved in disease progression. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated its efficacy in inhibiting protein-protein interactions critical for cancer cell survival. The compound's unique structural features allow for precise modifications, enhancing its binding affinity and selectivity.

N-Boc-N-bis(PEG1-OH), on the other hand, is a versatile building block in the synthesis of PEGylated compounds. Its bifunctional nature, featuring both a Boc-protected amine and hydroxyl-terminated PEG chains, makes it invaluable for creating biocompatible conjugates. A recent publication in Bioconjugate Chemistry highlighted its use in developing next-generation antibody-drug conjugates (ADCs), where it improved solubility and reduced immunogenicity. The study reported a 40% increase in therapeutic index compared to traditional linkers, underscoring its potential in ADC optimization.

In addition to therapeutic applications, 275385-03-0 has shown promise in diagnostic tools. A 2024 study in Analytical Chemistry utilized the compound as a fluorescent probe for detecting reactive oxygen species (ROS) in live cells. The probe's high sensitivity and specificity enabled real-time monitoring of oxidative stress, offering insights into neurodegenerative diseases. Similarly, N-Boc-N-bis(PEG1-OH) has been employed in the fabrication of nanocarriers for targeted drug delivery. Research in Nano Letters demonstrated its role in enhancing the stability and circulation time of liposomal formulations, achieving a 60% reduction in off-target effects.

The synthesis and scalability of these compounds have also been a focus of recent investigations. Advances in green chemistry have led to more efficient production methods for 275385-03-0, reducing the reliance on hazardous reagents. A 2023 patent application detailed a novel catalytic process that achieved a 90% yield with minimal waste. For N-Boc-N-bis(PEG1-OH), innovations in solid-phase synthesis have streamlined its production, as reported in Organic Process Research & Development. These developments are critical for meeting the growing demand in both academic and industrial settings.

Despite these advancements, challenges remain. The pharmacokinetic properties of 275385-03-0-derived compounds require further optimization to mitigate rapid clearance in vivo. Similarly, the cost-effectiveness of large-scale N-Boc-N-bis(PEG1-OH) production needs to be addressed to facilitate broader adoption. Collaborative efforts between academia and industry are essential to overcome these hurdles and fully realize the potential of these molecules.

In conclusion, 275385-03-0 and N-Boc-N-bis(PEG1-OH) represent cutting-edge tools in chemical biology and pharmaceutical research. Their diverse applications, from drug development to diagnostics, underscore their versatility and importance. Continued research and innovation will undoubtedly unlock new opportunities, paving the way for groundbreaking therapies and technologies.

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