tert-Butyl hydroxycarbamate

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

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

Name	tert-Butyl N-hydroxycarbamate
Synonym	More Synonyms

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

tert-Butyl hydroxycarbamate MSDS(Chinese)

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

Precursor 7
CAS#:24424-99-5 Di-tert-butyl d... CAS#:1070-19-5 Carbonazidic ac... CAS#:5470-11-1 Hydroxyamine hy... CAS#:24424-95-1 bis[(2-methylpr...
CAS#:870-46-2 tert-Butyl carbazate CAS#:31583-38-7 tert-butyl 1,4-... CAS#:105340-85-0 tert-Butyl benz...
DownStream 10
CAS#:105838-14-0 N-Boc-O-tosyl h... CAS#:110590-29-9 TERT-BUTYL 2-OX... CAS#:36016-39-4 tert-Butyl [(me... CAS#:35418-16-7 (S)-tert-Butyl ...
CAS#:144751-62-2 tert-butyl N-(o... CAS#:42989-85-5 (Boc-aminooxy)a... CAS#:20646-60-0 tert-butyl azep... CAS#:19689-97-5 TERT-BUTYL HYDR...
CAS#:85006-25-3 N,O-Di-Boc-hydr... CAS#:66605-57-0 N-Boc-L-phenyla...

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%

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...

(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

tert-Butyl hydroxycarbamate

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