Weight | 117.148 g/mol |
---|---|
Formula | C5H11NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
tert-Butyl carbamate (4248-19-5)
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- tert-Butyl [[2-(trimethylsilyl)ethyl]sulfonyl]carbamate : a new reagent for use in Mitsunobu reactions (Journal of Organic Chemistry, 1993)
- Conversion of primary amines to carbamate esters using palladium chloride and di-tert-butyl peroxide. Double carbonylation of secondary amines (Organometallics, 1987)
- Room-Temperature Pd-Catalyzed Amidation of Aryl Bromides Using tert-Butyl Carbamate (Journal of Organic Chemistry, 2009)
- Unexpected enantioseparation of mandelic acids and their derivatives on 1,2,3-triazolo-linked quinine tert-butyl carbamate anion exchange-type chiral stationary phase. (Journal of Separation Science, 2010)
- Pd-catalyzed amidation of aryl(Het) halides with tert-butyl carbamate (Tetrahedron Letters, 2010)
- One-pot three-component synthesis of tetrasubstituted NH pyrroles from secondary propargylic alcohols, 1,3-dicarbonyl compounds and tert-butyl carbamate (Journal of Heterocyclic Chemistry, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)OC(=O)N
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InChIKeyLFKDJXLFVYVEFG-UHFFFAOYSA-N
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