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150533

Sigma-Aldrich

Thallium(III) trifluoroacetate

technical grade

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Synonym(s):
TTFA, Tris(trifluoroacetato)thallium, Thallic trifluoroacetate, Trifluoroacetic acid thallium(III) salt
Linear Formula:
(CF3COO)3Tl
CAS Number:
Molecular Weight:
543.43
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Quality Level

reaction suitability

core: thallium
reagent type: catalyst

mp

213 °C (dec.) (lit.)

storage temp.

2-8°C

SMILES string

FC(F)(F)C(=O)O[Tl](OC(=O)C(F)(F)F)OC(=O)C(F)(F)F

InChI

1S/3C2HF3O2.Tl/c3*3-2(4,5)1(6)7;/h3*(H,6,7);/q;;;+3/p-3

InChI key

PSHNNUKOUQCMSG-UHFFFAOYSA-K

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This Item
14765155349163015
Thallium(III) trifluoroacetate technical grade

150533

Thallium(III) trifluoroacetate

Thallium(I) acetate purum, ≥97.0%

14765

Thallium(I) acetate

Thallium(I) cyclopentadienide 97%

155349

Thallium(I) cyclopentadienide

Thallium(III) nitrate trihydrate

163015

Thallium(III) nitrate trihydrate

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

-

storage temp.

2-8°C

storage temp.

-

mp

213 °C (dec.) (lit.)

mp

-

mp

300 °C (lit.)

mp

102-105 °C (lit.)

grade

technical grade

grade

-

grade

-

grade

-

Application

Oxidizing agent used in the synthesis of S-substituted cysteine peptides and proteins containing disulfide bonds.

signalword

Danger

Hazard Classifications

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

Storage Class

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Shenglong Zhu et al.
Nutrition and cancer, 72(4), 696-707 (2019-07-30)
Kudingcha is implicated in alleviating metabolic disorders in traditional Chinese medicine. However, the role of Kudingcha, one of the Ligustrum robustum species, in metabolic regulations and its antitumor activity in triple-negative breast cancer (TNBC) remains to be determined. Two breast
Cuihua Hu et al.
Molecular pharmaceutics, 16(2), 561-572 (2018-12-29)
The chimeric peptide HPRP-A1-iRGD, composed of a chemically conjugated tumor-homing/penetration domain (iRGD) and a cationic anticancer peptide domain (HPRP-A1), was used to study the effect of targeted modification to enhance the peptide's specificity, penetration, and tumor accumulation ability. The iRGD
Journal of the Chemical Society. Chemical Communications, 163-163 (1987)
Deacon, G. B.; Smith, R. N. M.
Journal of Fluorine Chemistry, 15, 85-85 (1980)
Tetrahedron, 44, 805-805 (1988)

Articles

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

Protocols

Overcome challenges in synthesis and disulfide bond formation with protocols for Fmoc solid-phase peptide synthesis of peptides with cysteine and methionine.

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