tert-Butyl carbamate
ALDRICH/167398 - 98%
Synonym: Boc-amide
CAS Number: 4248-19-5
Empirical Formula (Hill Notation): C5H11NO2
Molecular Weight: 117.15
EC Number: 224-209-3
MDL Number: MFCD00007962
Linear Formula: NH2COOC(CH3)3
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 167398-5G.
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 167398-100G
| assay | 98% |
| form | solid |
| InChI | 1S/C5H11NO2/c1-5(2,3)8-4( |
| InChI key | LFKDJXLFVYVEFG-UHFFFAOYSA |
| mp | 105-108 °C (lit.) |
| Quality Level | 200  |
| SMILES string | CC(C)(C)OC(N)=O |
| Application: | tert-Butyl carbamate was used in palladium-catalyzed synthesis of N-Boc-protected anilines. It was used in the synthesis of tetrasubstituted pyrroles, functionalized with ester or ketone groups at C-3 position. |
| General description: | Palladium-catalyzed cross-coupling reaction of tert-butyl carbamate with various aryl(Het) halides with Cs2CO3 as base in 1,4-dioxane (solvent) has been investigated. |
| Packaging: | 1, 5, 25, 100 g in glass bottle |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | 98% |
| mp | 105-108 °C (lit.) |
| UNSPSC | 12352100 |