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Merck
CN

163015

Thallium(III) nitrate trihydrate

Synonym(s):

TTN, Thallium trinitrate

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About This Item

Linear Formula:
Tl(NO3)3 · 3H2O
CAS Number:
Molecular Weight:
444.44
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
237-325-4
MDL number:
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InChI key

ZCPIKMRXMBJLCP-UHFFFAOYSA-N

InChI

1S/3NO3.3H2O.Tl/c3*2-1(3)4;;;;/h;;;3*1H2;/q3*-1;;;;+3

SMILES string

O.O.O.[Tl+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O

reaction suitability

core: thallium, reagent type: catalyst

mp

102-105 °C (lit.)

Quality Level

Application

Reagent for the rapid oxidation of styrene derivatives to carbonyl compounds, for the regioselective ring expansion of cyclic aralkyl ketones via oxidative rearrangement, for the selective hydrolysis of thioacetals to carbonyl compounds and for a general synthetic method to 19-norsteroids. Mediates ring contraction of cyclic ketones to a series of trans-fused 10-methyl-2-decalones.

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Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - STOT RE 2

Storage Class

5.1B - Oxidizing hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

危险化学品
铊类化学品
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Journal of the Chemical Society. Chemical Communications, 1026-1026 (1990)
Journal of the American Chemical Society, 98, 3037-3037 (1976)
Hyung Jun Park et al.
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To understand the characteristics of ADSSL1 myopathy, we investigated the clinical manifestation in Korean patients with ADSSL1 mutations. We developed a targeted panel of 16 distal-myopathy genes and recruited a total of 12 patients with genetically undetermined distal myopathy. We
Ferraz, H.M.C. Silva, L.F., Jr.
The Journal of Organic Chemistry, 63, 1716-1716 (1998)
Mathieu Cerino et al.
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Hereditary inclusion body myopathy (hIBM) refers to a group of clinically and genetically heterogeneous diseases. The overlapping histochemical features of hIBM with other genetic disorders lead to low diagnostic rates with targeted single-gene sequencing. This is true for the most

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Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis

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