| Identification | More | [Name]
N-Hydroxyurethane | [CAS]
589-41-3 | [Synonyms]
ETHYL HYDROXYCARBAMATE
ETHYL N-HYDROXYCARBAMATE
HYDROXYCARBAMIC ACID ETHYL ESTER
N-HYDROXYURETHAN
N-HYDROXYURETHANE
Ethylester kyseliny N-hydroxykarbaminove
ethylesterkyselinyn-hydroxykarbaminove
hydroxy-carbamicaciethylester
Hydroxyurethane
N-Carbethoxyhydroxylamine
NHU
N-Hydroxy ethyl carbamate
n-hydroxyethylcarbamate
NSC-71045
NSC-83629
SQ 16819
N-HYDROXYURETHAN 94+%
Ethyl hydroxycarbamate 97%
HYDROXYURETHAN
N-Hydroxycarbamic acid ethyl | [EINECS(EC#)]
209-648-0 | [Molecular Formula]
C3H7NO3 | [MDL Number]
MFCD00002108 | [Molecular Weight]
105.09 | [MOL File]
589-41-3.mol |
| Safety Data | Back Directory | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
2
| [RTECS ]
FB1750000
| [HS Code ]
2928009090 | [Toxicity]
LD50 intraperitoneal in rat: 800mg/kg |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow Oil | [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
| [Uses]
Hydroxyurethane is a metabolite of carcinogenic Urethane (U825300). | [Uses]
Metabolite of carcinogenic Urethane (U825300). | [Biochem/physiol Actions]
N-Hydroxyurethane causes the chromosomal fragmentation at millimolar concentrations and cell toxicity in cultured normal human leukocytes. |
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