o-allylhydroxylamine hydrochloride

Names

[ CAS No. ]:
206557-03-1

[ Name ]:
o-allylhydroxylamine hydrochloride

[Synonym ]:
MFCD00150102
O-Allylhydroxylamine hydrochloride hydrate

Chemical & Physical Properties

[ Boiling Point ]:
265.2ºC at 760 mmHg

[ Melting Point ]:
175ºC (dec.)(lit.)

[ Molecular Formula ]:
C₃H₁₀ClNO₂

[ Molecular Weight ]:
127.57000

[ Flash Point ]:
114.2ºC

[ Exact Mass ]:
127.04000

[ PSA ]:
44.48000

[ LogP ]:
1.50070

[ Vapour Pressure ]:
0.00211mmHg at 25°C

[ Water Solubility ]:
methanol: soluble25mg/mL, clear, colorless

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C

[ Risk Phrases ]:
34

[ Safety Phrases ]:
26-27-28-36/37/39-45

[ RIDADR ]:
UN 3263 8/PG 2

[ HS Code ]:
2922199090

Customs

[ HS Code ]: 2922199090

[ Summary ]:
2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Antiviral and tumor cell antiproliferative SAR studies on tetracyclic eudistomins. II.

Bioorg. Med. Chem. 5(5) , 955-70, (1997)

In a search for the minimum pharmacophore of the naturally occurring tetracyclic eudistomins, five structural analogues (4-8) were evaluated for their in vitro antiviral and tumor cell antiproliferati...

Synthesis of (R)-{η 6-[O-methyl-N-(α-methylbenzyl) hydroxyamino] benzene} chromium tricarbonyl via nucleophilic aromatic substitution of (η 6-fluorobenzene) chromium tricarbonyl. da Costa MRG, et al.

J. Chem. Soc. Perkin Trans. I 21 , 2850-55, (2001)

O-Allylhydroxylamine Hydrochloride
N-benzyl O-allylhydroxylamine
N-benzyl-N-phenyl-O-allylhydroxylamine
O-Allyl-hydroxylamine
O-allyl-N-(α-methylbenzyl)hydroxylamine
N-prop-2-enoxybenzamide
N-(2,3-dimethoxybenzyl)-2-(2-(3-ethylphenyl)-1,1-dioxido-3-oxo-2H-benzo[e][1,2,4]thiadiazin-4(3H)-yl)acetamide
N-(2,3-dimethoxybenzyl)-2-(2-(2,5-dimethylphenyl)-1,1-dioxido-3-oxo-2H-benzo[e][1,2,4]thiadiazin-4(3H)-yl)acetamide
N-(2,3-dimethoxybenzyl)-2-(2-(3-methoxyphenyl)-1,1-dioxido-3-oxo-2H-benzo[e][1,2,4]thiadiazin-4(3H)-yl)acetamide
8-Methyl-3-(piperazin-1-yl)-8-azabicyclo[3.2.1]octane
N-(2,4-dichlorobenzyl)-4-(1,1-dioxido-2H-benzo[e][1,2,4]thiadiazin-3-yl)-3-methylbutanamide
N-benzyl-3-[5-({[(4-ethoxyphenyl)carbamoyl]methyl}sulfanyl)-3-oxo-2H,3H-imidazo[1,2-c]quinazolin-2-yl]propanamide
N-benzyl-3-[5-({[(2,5-dimethoxyphenyl)carbamoyl]methyl}sulfanyl)-3-oxo-2H,3H-imidazo[1,2-c]quinazolin-2-yl]propanamide
2-(3,5-dimethoxyphenyl)-4-(2-(4-fluorophenyl)-2-oxoethyl)-2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide
N-[(4-methoxyphenyl)methyl]-3-[5-({[(3-methoxypropyl)carbamoyl]methyl}sulfanyl)-3-oxo-2H,3H-imidazo[1,2-c]quinazolin-2-yl]propanamide
3-{5-[({[4-(dimethylamino)phenyl]carbamoyl}methyl)sulfanyl]-3-oxo-2H,3H-imidazo[1,2-c]quinazolin-2-yl}-N-[(2-methoxyphenyl)methyl]propanamide

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