CAS 36016-38-3|tert-Butyl hydroxycarbamate
Introduction：Basic information about CAS 36016-38-3|tert-Butyl hydroxycarbamate, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | tert-Butyl hydroxycarbamate | ||
|---|---|---|---|
| CAS Number | 36016-38-3 | Molecular Weight | 133.146 |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 250.4±9.0 °C at 760 mmHg |
| Molecular Formula | C5H11NO3 | Melting Point | 53-55 °C(lit.) |
| MSDS | ChineseUSA | Flash Point | 105.2±18.7 °C |
Names
| Name | tert-Butyl N-hydroxycarbamate |
|---|---|
| Synonym | More Synonyms |
Chemical & Physical Properties
| Density | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 250.4±9.0 °C at 760 mmHg |
| Melting Point | 53-55 °C(lit.) |
| Molecular Formula | C5H11NO3 |
| Molecular Weight | 133.146 |
| Flash Point | 105.2±18.7 °C |
| Exact Mass | 133.073898 |
| PSA | 58.56000 |
| LogP | 0.82 |
| Vapour Pressure | 0.0±1.1 mmHg at 25°C |
| Index of Refraction | 1.443 |
| InChIKey | DRDVJQOGFWAVLH-UHFFFAOYSA-N |
| SMILES | CC(C)(C)OC(=O)NO |
| Storage condition | 2-8°C |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| Safety Phrases | S22-S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 29280090 |
Customs
| HS Code | 2924199090 |
|---|---|
| Summary | 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Articles10
More Articles| N-O chemistry for antibiotics: discovery of N-alkyl-N-(pyridin-2-yl)hydroxylamine scaffolds as selective antibacterial agents using nitroso Diels-Alder and ene chemistry. J. Med. Chem. 54 , 6843-58, (2011) The discovery, syntheses, and structure-activity relationships (SAR) of a new family of heterocyclic antibacterial compounds based on N-alkyl-N-(pyridin-2-yl)hydroxylamine scaffolds are described. A s... | |
| Prodrugs of nitroxyl as inhibitors of aldehyde dehydrogenase. J. Med. Chem. 35 , 3648, (1992) In the preceding paper, analogs of chlorpropamide with an OMe substituent on the sulfonamide nitrogen were shown to inhibit aldehyde dehydrogenase (AlDH), and it was postulated that these compounds we... | |
| Reactions of nitroso hetero-Diels-Alder cycloadducts with azides: stereoselective formation of triazolines and aziridines. J. Org. Chem. 72 , 3929, (2007) The addition of azides to acylnitroso hetero-Diels-Alder cycloadducts derived from cyclopentadiene affords exo-triazolines in excellent yield. The reaction is greatly affected by the level of alkene s... |
Synonyms
| (tert-butyl)oxycarbohydroxamic acid |
| N-(tert-Butoxycarbonyl)hydroxylamine |
| tert-butyl N-hydroxy-carbamate |
| N-tert-Butoxycarbonylhydroxylamine |
| MFCD00002107 |
| tert-Butyl hydroxycarbamate |
| t-Butyl N-hydroxycarbamate |
| EINECS 252-836-2 |
| N-Boc-hydroxylamine |
| 1,1-dimethylethyl N-hydroxycarbamate |
| N-Hydroxycarbamic Acid tert-Butyl Ester |
| 2-Methyl-2-propanyl hydroxycarbamate |
| N-(t-Butoxycarbonyl)-hydroxylamine |
| Carbamic acid, N-hydroxy-, 1,1-dimethylethyl ester |
