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Molecular structure of 2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol, CAS Number: 139115-92-7
2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol (CAS 139115-92-7)
Alternate Names:
N-[2-[2-(2-Hydroxyethoxy)ethoxy]ethyl]carbamic Acid 1,1-Dimethylethyl Ester; 2-[2-(2-tert-Butyloxycarbonylaminoethoxy)ethoxy]ethanol
Application:
2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol is a cross-linking reagent
CAS Number:
139115-92-7
Molecular Weight:
249.30
Molecular Formula:
C11H23NO5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol, also known as, 2-[2-(2-tert-Butyloxycarbonylaminoethoxy)ethoxy]ethanol, is a cross-linking reagent. The compound has been used to study novel RGD-like molecules with a tyrosine template. In addition, 2-[2-(2-tert-Butyloxycarbonylaminoethoxy)ethoxy]ethanol was used to synthesize peptidomimetics with a spacer-arm.
2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol (CAS 139115-92-7) References
- Novel RGD-like molecules based on the tyrosine template: design, synthesis, and biological evaluation on isolated integrins alphaVbeta3/alphaIIbbeta3 and in cellular adhesion tests. | Biltresse, S., et al. 2004. Bioorg Med Chem. 12: 5379-93. PMID: 15388165
- Structure-based hybridization of the bioactive natural products rhizonin A and ternatin leading to a selective fat-accumulation inhibitor against 3T3-L1 adipocytes. | Shimokawa, K., et al. 2009. Bioorg Med Chem Lett. 19: 867-9. PMID: 19097891
- Synthesis and biological evaluation of berberine derivatives as a new class of broad-spectrum antiviral agents against Coxsackievirus B. | Zeng, QX., et al. 2020. Bioorg Chem. 95: 103490. PMID: 31855821
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol, 250 mg | sc-208968 | 250 mg | $305.00 |