Weight | 117.148 g/mol |
---|---|
Formula | C5H11NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
Butyl carbamate (592-35-8)
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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)
- Homogeneous phase synthesis of cellulose carbamate silica hybrid materials using 1-n-butyl-3-methylimidazolium chloride ionic liquid medium (Carbohydrate Polymers, 2009)
- Cholesteric Mesophases Formed by the Modified Biological Macromolecule 3,6-O-(Butyl Carbamate)-N-phthaloyl Chitosan (Macromolecules, 1994)
- ASYMMETRIC AMINOHYDROXYLATION OF SUBSTITUTED STYRENES USING T-BUTYL CARBAMATE (Tetrahedron Letters, 1998)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCOC(=O)N
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InChIKeySKKTUOZKZKCGTB-UHFFFAOYSA-N
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