O-Tritylhydroxylamine
Suppliers
Names
[ CAS No. ]:
31938-11-1
[ Name ]:
O-Tritylhydroxylamine
[Synonym ]:
O-triphenylmethyloxyamine
O-(Triphenylmethyl)hydroxylamine
EINECS 250-868-1
O-Tritylhydroxylamine
triphenylmethoxyamine
Trityloxyamine
MFCD00042818
Hydroxylamine, O-(triphenylmethyl)-
Trityl-O-Hydroxylamine
NH2-O-trityl
1,1',1''-[(Aminooxy)methanetriyl]tribenzene
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
443.2±44.0 °C at 760 mmHg
[ Melting Point ]:
79-81ºC(lit.)
[ Molecular Formula ]:
C19H17NO
[ Molecular Weight ]:
275.344
[ Flash Point ]:
235.1±22.1 °C
[ Exact Mass ]:
275.131012
[ PSA ]:
35.25000
[ LogP ]:
5.15
[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C
[ Index of Refraction ]:
1.616
[ Storage condition ]:
2-8°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
36/37/38
[ Safety Phrases ]:
26-37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2922199090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
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
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There are many of pathogen parasite species with different susceptibility profile to antiparasitic drugs. Unfortunately, almost QSAR models predict the biological activity of drugs against only one pa...
Bioorg. Med. Chem. 18(1) , 415-25, (2010)
Histone deacetylase inhibitors (HDACi) are endowed with plethora of biological functions including anti-proliferative, anti-inflammatory, anti-parasitic, and cognition-enhancing activities. Parsing th...
Bioorg. Med. Chem. Lett. 19(23) , 6588-90, (2009)
We describe herein the synthesis and characterization of a new class of histone deacetylase (HDAC) inhibitors derived from conjugation of a suberoylanilide hydroxamic acid-like aliphatic-hydroxamate p...