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

2-(tert-Butoxycarbonylamino)-1-ethanol

CAS: 26690-80-2

Formula: C₇H₁₅NO₃

Purity: >98.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 161.20

Ref: 3B-H0899

2-(Boc-amino)ethanol, 95%

CAS: 26690-80-2

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.

Formula: C₇H₁₅NO₃

Purity: 95%

Color and Shape: Liquid or viscous liquid, Clear colorless

Molecular weight: 161.20

Ref: 02-H32356

Boc-NH-PEG1-OH

CAS: 26690-80-2

Boc-NH-PEG1-OH

Formula: C₇H₁₅NO₃

Purity: ≥98%

Molecular weight: 161.2

Ref: 54-BUP19654

2-Aminoethan-1-ol, N-BOC protected

CAS: 26690-80-2

2-Aminoethan-1-ol, N-BOC protected

Formula: C₇H₁₅NO₃

Purity: ≥95%

Color and Shape: Liquid-Viscous

Molecular weight: 161.19889

Ref: 54-OR70054

tert-Butyl N-(2-hydroxyethyl)carbamate

CAS: 26690-80-2

Formula: C₇H₁₅NO₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 161.1989

Ref: IN-DA0035NA

tert-Butyl N-(2-hydroxyethyl)carbamate

CAS: 26690-80-2

Formula: C₇H₁₅NO₃

Molecular weight: 161.20

Ref: 7W-GK9775

N-Boc-Ethanolamine

CAS: 26690-80-2

Formula: C₇H₁₅NO₃

Purity: 97%

Color and Shape: Viscous Liquid, Clear or Viscous Liquid

Molecular weight: 161.201

Ref: 10-F022129

Boc-NH-PEG1-OH

CAS: 26690-80-2

tert-Butyl (2-hydroxyethyl)carbamate

Formula: C₇H₁₅NO₃

Purity: 98%

Molecular weight: 161.2

Ref: IN-DG10099

Ethanolamine Impurity 1

CAS: 26690-80-2

Formula: C₇H₁₅NO₃

Molecular weight: 161.20

Ref: 4Z-E-184001

Boc-NH-PEG1-OH

CAS: 26690-80-2

Boc-NH-PEG1-OH is a PEG-based PROTAC linker that can be used in PROTAC synthesis.

Formula: C₇H₁₅NO₃

Purity: 99.32%

Color and Shape: Solid

Molecular weight: 161.2

Ref: TM-T17659

N-Boc-ethanolamine

Controlled Product

CAS: 26690-80-2

Applications N-Boc-ethanolamine (cas# 26690-80-2) is a compound useful in organic synthesis.
References Snead, A., et al.: Bioorg. Med. Chem. Lett., 18, 5920 (2008),

Formula: C₇H₁₅NO₃

Color and Shape: Neat

Molecular weight: 161.2

Ref: TR-B649490

N-Boc-ethanolamine

CAS: 26690-80-2

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).

Formula: C₇H₁₅NO₃

Purity: Min. 95%

Color and Shape: Colorless Clear Liquid

Molecular weight: 161.2 g/mol

Ref: 3D-FB18941

N-Boc-ethanolamine

CAS: 26690-80-2

Formula: C₇H₁₅NO₃

Molecular weight: 161.2

Ref: ST-EA-CP-A5018