| Weight | 223.272 g/mol |
|---|---|
| Formula | C12H17NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
tert-butyl benzyloxycarbamate (79722-21-7)
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LabBot
- Phase-transfer catalytic aza-Michael addition of tert-butyl benzyloxycarbamate to electron-deficient olefins (Chemical Communications, 2008)
- ChemInform Abstract: PhaseTransfer Catalytic AzaMichael Addition of tertButyl Benzyloxycarbamate to ElectronDeficient Olefins. (ChemInform, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)OC(=O)NOCC1=CC=CC=C1
-
InChIKeyMZNBNPWFHGWAGH-UHFFFAOYSA-N
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Alternate Names
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Synthesis
Reactant
+
O-Benzylhydroxylamine
(Schotten-Baumann amide from acid)
Reactant
+
2-Chloro-2-methylpropane
(Ester from carboxilic acid(SN2))
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tert-butyl benzyloxycarbamate
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