tert-Butyl hydroxycarbamate structure
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Common Name | tert-Butyl hydroxycarbamate | ||
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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 | Chinese USA | Flash Point | 105.2±18.7 °C |
Name | tert-Butyl N-hydroxycarbamate |
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Synonym | More Synonyms |
Density | 1.1±0.1 g/cm3 |
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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 |
Storage condition | 2-8°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 29280090 |
Precursor 7 | |
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DownStream 10 | |
HS Code | 2924199090 |
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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% |
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... |
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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... |
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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... |
(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 |