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N-Hydroxyurethane

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N-Hydroxyurethane Basic information

Product Name:
N-Hydroxyurethane
Synonyms:
  • ETHYL HYDROXYCARBAMATE
  • ETHYL N-HYDROXYCARBAMATE
  • HYDROXYCARBAMIC ACID ETHYL ESTER
  • Ethylester kyseliny N-hydroxykarbaminove
  • Ethyl Hydroxycarbamate Hydroxycarbamic Acid Ethyl Ester
  • N-Hydroxyurethane
  • ethylesterkyselinyn-hydroxykarbaminove
  • hydroxy-carbamicaciethylester
CAS:
589-41-3
MF:
C3H7NO3
MW:
105.09
EINECS:
209-648-0
Product Categories:
  • Amines
  • Mutagenesis Research Chemicals
  • Aliphatics
  • Hydroxylamines
  • Hydroxylamines (N-Substituted)
Mol File:
589-41-3.mol
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N-Hydroxyurethane Chemical Properties

Boiling point:
113-116 °C3 mm Hg(lit.)
Density 
1.3895 (rough estimate)
refractive index 
n20/D 1.445(lit.)
Flash point:
>230 °F
storage temp. 
-20°C
solubility 
Diethyl Ether, Dimethyl Sulfoxide, Water
form 
Oil
pka
9.30±0.23(Predicted)
color 
Yellow
BRN 
1747529
CAS DataBase Reference
589-41-3(CAS DataBase Reference)
NIST Chemistry Reference
Carbamic acid, hydroxy-, ethyl ester(589-41-3)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
2
RTECS 
FB1750000
HS Code 
2928009090
Toxicity
LD50 intraperitoneal in rat: 800mg/kg

MSDS

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N-Hydroxyurethane Usage And Synthesis

Chemical Properties

Yellow Oil

Uses

Hydroxyurethane is a metabolite of carcinogenic Urethane (U825300).

Uses

Reactant involved in:

  • Synthesis of molecules used for intermolecular Sharpless aminohydroxylation reactions
  • Intermolecular ortho-C-H amidation of anilides
  • Cinchona alkaloid-catalyzed asymmetric cycloaddition
  • Allylic arylation

Biochem/physiol Actions

N-Hydroxyurethane causes the chromosomal fragmentation at millimolar concentrations and cell toxicity in cultured normal human leukocytes.

N-HydroxyurethaneSupplier

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