| Identification | More | [Name]
BENZYL N-(2-HYDROXYETHYL)CARBAMATE | [CAS]
77987-49-6 | [Synonyms]
Z-GLY-OL
Z-GLYCINOL
Cbz-Gly-OL
Z-NH-(CH2)2-OH
Z-AMINOETHANOL
Z-ETHANOLAMINE
N-CBZ-GLYCINOL
N-Z-ETHANOLAMINE
2-(Z-AMINO)-ETHANOL
2-(Cbz-amino)ethanol
N-Z-EthanolaMine 98%
LABOTEST-BB LT00452296
Z-Glycinol≥ 99% (HPLC)
2-(CBZ-AMINO)-1-ETHANOL
N-CARBOBENZOXY-GLYCINOL
N-CARBOBENZOXY-2-AMINOETHANOL
2-(CARBOBENZOXYAMINO)-1-ETHANOL
Benzyl (2-hydroxyethyl)carbaMate
2-(Carbobenzoxyamino)-1-ethanol>
BENZYL N-(2-HYDROXYETHYL)CARBAMATE
2-(Benzyloxycarbonylamino)-1-ethanol
N - (benzyloxycarbonylamino) - 1-ethanol
(2-Hydroxy-ethyl)-carbamic acid benzyl ester
BENZYL N-(2-HYDROXYETHYL)CARBAMATE USP/EP/BP
N-(2-HYDROXYETHYL)CARBAMIC ACID BENZYL ESTER
N-(2-hydroxyethyl)carbamic acid (phenylmethyl) ester
Carbamic acid, N-(2-hydroxyethyl)-, phenylmethyl ester
2-(Z-Amino)ethanol, Benzyl N-(2-hydroxyethyl)carbamate
Benzyl N-(2-Hydroxyethyl)carbamate
2-(Cbz-amino)-1-ethanol
N-(2-Hydroxyethyl)carbamic Acid Benzyl Ester | [EINECS(EC#)]
629-174-1 | [Molecular Formula]
C10H13NO3 | [MDL Number]
MFCD00191060 | [Molecular Weight]
195.22 | [MOL File]
77987-49-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
58-60 °C (lit.) | [Boiling point ]
215 °C/15 mmHg (lit.) | [density ]
1.1926 (rough estimate) | [refractive index ]
1.5150 (estimate) | [storage temp. ]
Store at 0-5°C | [solubility ]
Soluble in water or 1% acetic acid | [form ]
Powder | [pka]
11.80±0.46(Predicted) | [color ]
White | [BRN ]
2050891 | [CAS DataBase Reference]
77987-49-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [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:Wear suitable protective clothing . | [WGK Germany ]
3
| [HS Code ]
29221985 |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
N-(Benzyloxycarbonyl)ethanolamine is an intermediate used to prepare alkynylaryladenines as A2A adenosine receptor agonists and effects on hepatic glucose production. It is also used in the synthesis of functionalized N-arylaminoethyl amides as noncovalent inhibitors of cathepsin S. | [reaction suitability]
reagent type: cross-linking reagent |
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