tert-Butyl hydroxycarbamate

Modify Date: 2024-01-02 19:42:47

tert-Butyl hydroxycarbamate Structure
tert-Butyl hydroxycarbamate structure
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 Chinese USA 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
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
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