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TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE

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CAS:26690-80-2
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  • 2026-02-26
  • CAS:26690-80-2
  • Min. Order: 1kg
  • Purity: 98%
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TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE Basic information
Product Name:TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE
Synonyms:2-(TERT-BUTOXYCARBONYLAMINO)-1-ETHANOL;(2-HYDROXY-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER;2-(BOC-AMINO)-1-ETHANOL;N-T-BUTOXYCARBONYL-2-AMINOETHANOL;N-T-BUTOXYCARBONYL-GLYCINOL;N-(TERT-BUTOXYCARBONYL)ETHANOLAMINE;N-(2-HYDROXYETHYL)CARBAMIC ACID TERT-BUTYL ESTER;N-(2-HYDROXYMETHYL)CARBAMIC ACID BENZYL ESTER
CAS:26690-80-2
MF:C7H15NO3
MW:161.2
EINECS:675-176-0
Product Categories:Amines;Miscellaneous Reagents;Amino Alcohols;Boc-Amino acid series;Amino Acids;Miscellaneous Natural Products
Mol File:26690-80-2.mol
TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE Structure
TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE Chemical Properties
Boiling point 92℃/0.22mm
density 1.042 g/mL at 25 °C(lit.)
refractive index n20/D 1.449(lit.)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Sparingly), Methanol (Slightly)
pka12.01±0.46(Predicted)
form viscous liquid
color clear, light yellow
Specific Gravity1.042
Water Solubility Soluble in water or 1% acetic acid. Soluble in ethyl acetate and methanol.
BRN 2353995
InChIInChI=1S/C7H15NO3/c1-7(2,3)11-6(10)8-4-5-9/h9H,4-5H2,1-3H3,(H,8,10)
InChIKeyGPTXCAZYUMDUMN-UHFFFAOYSA-N
SMILESC(OC(C)(C)C)(=O)NCCO
CAS DataBase Reference26690-80-2(CAS DataBase Reference)
Safety Information
Hazard Codes T
Risk Statements 25-37/38-41-36/37/38-23/24/25
Safety Statements 26-39-45-36/37/39-37/39
RIDADR UN 2810 6.1/PG 3
WGK Germany 3
10-21
HazardClass IRRITANT
HS Code 29241990
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE Usage And Synthesis
Chemical PropertiesLight yellow clear liquid
Usessuzuki reaction
UsesAmine protected, difunctional reagent employed in the synthesis of phosphatidyl ethanolamines and ornithine.
Synthesis Reference(s)Tetrahedron Letters, 28, p. 4185, 1987 DOI: 10.1016/S0040-4039(00)95574-6
reaction suitabilityreagent type: cross-linking reagent
SynthesisTo the diethanolamine add benzyl chloride, heating to reflux state reaction 1 ~ 1.5h, cooled to 23 ~ 28 , add chlorosulfoxide, wait until the reaction is complete after the reaction through the liquid ammonia reaction 2.5 ~ 3.5h, cooled to 23 ~ 28 , add the di-tert-butyl dicarbonate stirring reaction 0.5 ~ 1h, through the hydrogen de-benzyl, that is, to obtain the product N-(tert-butoxycarbonyl)ethanolamine.
IC 50PEGs
Tag:TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE(26690-80-2) Related Product Information
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