CAS 26690-80-2
:N-(tert-Butoxycarbonyl)ethanolamine
Description:
N-(tert-Butoxycarbonyl)ethanolamine, with the CAS number 26690-80-2, is an organic compound characterized by the presence of both an amine and a carbonyl functional group. It features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during various chemical reactions. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents such as dichloromethane and methanol, but its solubility in water is limited due to the hydrophobic tert-butyl group. The presence of the ethanolamine moiety imparts basic properties, allowing it to participate in various nucleophilic reactions. N-(tert-Butoxycarbonyl)ethanolamine is often utilized in peptide synthesis and other organic transformations, where the Boc group can be selectively removed under acidic conditions to regenerate the free amine. Safety data should be consulted for handling, as it may pose health risks if ingested or inhaled.
Formula:C7H15NO3
InChI:InChI=1/C7H15NO3/c1-7(2,3)11-6(10)8-4-5-9/h9H,4-5H2,1-3H3,(H,8,10)
SMILES:CC(C)(C)OC(=NCCO)O
Synonyms:- N-Boc-ethanolamine
- tert-Butyl N-(2-hydroxyethyl)carbamate
- N-BOC-Aminoethanol
- Boc-Glycinol
- N-(2-Hydroxymethyl)carbamic acid benzyl ester
- Tert-Butyl (2-Hydroxyethyl)Carbamate
- 2-(Boc-amino)-1-ethanol
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Found 12 products.
2-(tert-Butoxycarbonylamino)-1-ethanol
CAS:Formula:C7H15NO3Purity:>98.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:161.202-(Boc-amino)ethanol, 95%
CAS:<p>Suzuki reaction. 2-(Boc-amino)ethanol as reagent in Novel bisbenzimide-nitroxides for nuclear redox imaging in living cells. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand.</p>Formula:C7H15NO3Purity:95%Color and Shape:Liquid or viscous liquid, Clear colorlessMolecular weight:161.20tert-Butyl N-(2-hydroxyethyl)carbamate
CAS:Formula:C7H15NO3Purity:95%Color and Shape:LiquidMolecular weight:161.1989Ref: IN-DA0035NA
5g22.00€10g20.00€1kg164.00€25g26.00€50g32.00€5kg696.00€100g50.00€10kgTo inquire250g85.00€25kgTo inquire500g123.00€2-Aminoethan-1-ol, N-BOC protected
CAS:<p>2-Aminoethan-1-ol, N-BOC protected</p>Formula:C7H15NO3Purity:≥95%Color and Shape: clear. colourless high viscous liquidMolecular weight:161.19889g/molBoc-NH-PEG1-OH
CAS:<p>Boc-NH-PEG1-OH is a PEG-based PROTAC linker that can be used in PROTAC synthesis.</p>Formula:C7H15NO3Purity:99.32%Color and Shape:Clear Light Yellow Viscous LiquidMolecular weight:161.2N-Boc-Ethanolamine
CAS:Formula:C7H15NO3Purity:97%Color and Shape:Viscous Liquid, Clear or Viscous LiquidMolecular weight:161.201N-Boc-ethanolamine
CAS:Controlled Product<p>Applications N-Boc-ethanolamine (cas# 26690-80-2) is a compound useful in organic synthesis.<br>References Snead, A., et al.: Bioorg. Med. Chem. Lett., 18, 5920 (2008),<br></p>Formula:C7H15NO3Color and Shape:NeatMolecular weight:161.20N-Boc-ethanolamine
CAS:<p>N-Boc-ethanolamine is a naturally occurring antimicrobial peptide that has been shown to have an inhibitory effect on the growth of cancer cells in vitro. It also inhibits glucose production in the body and has been used in the treatment of diabetes mellitus. N-Boc-ethanolamine is synthesized by solid-phase synthesis with ferrocenecarboxylic acid, followed by reaction with aldehyde groups and subsequent hydrogenation. This compound has potent inhibition against cancer cells and can be used as a chemotherapeutic agent for cancer treatment. The hydrogen bond between this compound and β-unsaturated ketones leads to its photochemical properties. Cellular uptake of N-Boc-ethanolamine was observed when it was conjugated to polymers such as polyethylene glycol (PEG).</p>Formula:C7H15NO3Purity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:161.2 g/mol










