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Merck

358894

O-Tritylhydroxylamine

95%

Synonym(s):

O-(Triphenylmethyl)hydroxylamine, Trityloxyamine

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About This Item

Linear Formula:
(C6H5)3CONH2
CAS Number:
31938-11-1
Molecular Weight:
275.34
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24862034
EC Number:
250-868-1
Beilstein/REAXYS Number:
1983917
MDL number:
MFCD00042818

Key Documents

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Product Name

O-Tritylhydroxylamine, 95%

InChI key

NZFHJBSDSXDUAO-UHFFFAOYSA-N

InChI

1S/C19H17NO/c20-21-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H,20H2

SMILES string

NOC(c1ccccc1)(c2ccccc2)c3ccccc3

assay

95%

mp

79-81 °C (lit.)

functional group

phenyl

Quality Level

200

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Application

O-Tritylhydroxylamine may be used in the preparation of 8-azido-O-trityloctahydroxamate and 9-azido-O-tritylnonahydroxamate. It may be used in the synthesis of Simian virus nuclear localization peptide (NLS)-histone deacetylase (HDAC) inhibitor conjugates.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000247163
0000218005
0000247163
0000218005
0000144432

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Vishal Patil et al.
Bioorganic & medicinal chemistry, 18(1), 415-425 (2009-11-17)
Histone deacetylase inhibitors (HDACi) are endowed with plethora of biological functions including anti-proliferative, anti-inflammatory, anti-parasitic, and cognition-enhancing activities. Parsing the structure-activity relationship (SAR) for each disease condition is vital for long-term therapeutic applications of HDACi. We report in the present
Joshua C Canzoneri et al.
Bioorganic & medicinal chemistry letters, 19(23), 6588-6590 (2009-10-27)
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 pharmacophore to a nuclear localization signal peptide. We found that these conjugates inhibited the histone
Francisco J Prado-Prado et al.
Bioorganic & medicinal chemistry, 18(6), 2225-2231 (2010-02-27)
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 parasite species. Consequently, predicting the probability with which a drug is active against

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