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tert-Butyl carbazate, 98+%
CAS: 870-46-2 | C5H12N2O2 | 132.163 g/mol
$138.74 - $1101.55
Chemical Identifiers
| CAS | 870-46-2 |
|---|---|
| Molecular Formula | C5H12N2O2 |
| Molecular Weight (g/mol) | 132.163 |
| MDL Number | MFCD00007593 |
| InChI Key | DKACXUFSLUYRFU-UHFFFAOYSA-N |
| Synonym | tert-butyl carbazate, tert-butyl hydrazinecarboxylate, t-butyl carbazate, hydrazinecarboxylic acid, 1,1-dimethylethyl ester, t-butylcarbazate, tert-butoxycarbonyl hydrazide, boc-hydrazide, boc-hydrazine, tert-butoxycarbonyl hydrazine, carbazic acid tert-butyl ester |
| PubChem CID | 70091 |
| IUPAC Name | tert-butyl N-aminocarbamate |
| SMILES | CC(C)(C)OC(=O)NN |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1238314
|
Thermo Scientific Chemicals
A1238314 |
25 g |
Each for $138.74
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AAA1238322
|
Thermo Scientific Chemicals
A1238322 |
100 g |
Each for $273.62
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AAA1238336
|
Thermo Scientific Chemicals
A1238336 |
500 g |
Each for $1,101.55
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Description
tert-Butyl carbazate is used in a palladium-catalyzed cross-coupling with vinyl halides to prepare N-Boc-N-alkenylhydrazines. It is utilized in solid phase peptide synthesis and in the optical purity determination of alfa-amino aldehyde. It reacts with aldehydes to get hydrazones, which finds application as an intermediate in the synthesis of HIV-1 protease inhibitors. In addition to this, it is used as a starting material for the preparation of BOC-azide, sulfonic and carboxylic hydrazides.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applicationstert-Butyl carbazate is used in a palladium-catalyzed cross-coupling with vinyl halides to prepare N-Boc-N-alkenylhydrazines. It is utilized in solid phase peptide synthesis and in the optical purity determination of alfa-amino aldehyde. It reacts with aldehydes to get hydrazones, which finds application as an intermediate in the synthesis of HIV-1 protease inhibitors. In addition to this, it is used as a starting material for the preparation of BOC-azide, sulfonic and carboxylic hydrazides.
Solubility
Soluble in ethanol and methanol.
Notes
Store in a cool place. Incompatible with strong oxidizing agents and strong bases.
Chemical Identifiers
| 870-46-2 | |
| 132.163 | |
| DKACXUFSLUYRFU-UHFFFAOYSA-N | |
| 70091 | |
| CC(C)(C)OC(=O)NN |
| C5H12N2O2 | |
| MFCD00007593 | |
| tert-butyl carbazate, tert-butyl hydrazinecarboxylate, t-butyl carbazate, hydrazinecarboxylic acid, 1,1-dimethylethyl ester, t-butylcarbazate, tert-butoxycarbonyl hydrazide, boc-hydrazide, boc-hydrazine, tert-butoxycarbonyl hydrazine, carbazic acid tert-butyl ester | |
| tert-butyl N-aminocarbamate |
Specifications
| 870-46-2 | |
| 63°C to 65°C (0.1 mmHg) | |
| C5H12N2O2 | |
| 25 g | |
| 1756967 | |
| tert-butyl carbazate, tert-butyl hydrazinecarboxylate, t-butyl carbazate, hydrazinecarboxylic acid, 1,1-dimethylethyl ester, t-butylcarbazate, tert-butoxycarbonyl hydrazide, boc-hydrazide, boc-hydrazine, tert-butoxycarbonyl hydrazine, carbazic acid tert-butyl ester | |
| DKACXUFSLUYRFU-UHFFFAOYSA-N | |
| tert-butyl N-aminocarbamate | |
| 70091 | |
| ≥98% |
| 37°C to 41°C | |
| 91°C (195°F) | |
| MFCD00007593 | |
| UN1325 | |
| Moisture sensitive | |
| Soluble in ethanol and methanol. | |
| CC(C)(C)OC(=O)NN | |
| 132.163 | |
| 132.16 | |
| tert-Butyl carbazate |
Safety and Handling
GHS H Statement
H228
Flammable solid.
P210-P240-P241-P261-P264b-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P361-P363-P370+P378q-P501c
H228-H301+H311-H315-H319-H335
DOTInformation : Hazard Class: 4.1; Packaging Group: II
EINECSNumber : 212-795-3
TSCA : Yes
Recommended Storage : Keep cold
RUO – Research Use Only