O-Tritylhydroxylamine

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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

Click to get detail 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

Click to get detail 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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Bioorg. Med. Chem. 18 , 2225-31, (2010)

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...

Antimalarial and antileishmanial activities of histone deacetylase inhibitors with triazole-linked cap group.

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...

Design and synthesis of novel histone deacetylase inhibitor derived from nuclear localization signal peptide

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...

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O-(OCTYLPHOSPHORYL)CHOLINE SOLUTION