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Merck
CN

SML3521

m-Trifluoromethyl-diphenyl diselenide

≥98% (HPLC)

Synonym(s):

1,2-Bis(3-(trifluoromethyl)phenyl)diselane, Bis(3-trifluoromethylphenyl) diselenide, Di(3-trifluoromethylphenyl) diselenide, TFDD, [(m-CF3-PhSe)2; Bis[3-(trifluoromethyl)phenyl] diselenide

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About This Item

Empirical Formula (Hill Notation):
C14H8F6Se2
CAS Number:
Molecular Weight:
448.12
UNSPSC Code:
51111800
NACRES:
NA.25
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InChI key

DGOYKERNPXVRDM-UHFFFAOYSA-N

SMILES string

FC(F)(C1=CC([Se][Se]C2=CC=CC(C(F)(F)F)=C2)=CC=C1)F

assay

≥98% (HPLC)

form

oil

color

colorless to yellow

storage temp.

-10 to -25°C

Quality Level

Biochem/physiol Actions

Brain blood barrier penetrant organoselenium compound that exhibits antinociceptive and antidepressant effects
m-Trifluoromethyl-diphenyl diselenide (TFDD) is a brain blood barrier penetrant organoselenium compound that exhibits antinociceptive and antidepressant effects in animal models without development of tolerance or withdrawal sighs. m-Trifluoromethyl-diphenyl diselenide acts as opioid system modulator, which attenuates morphine withdrawal signs in mice. It exhibits antioxidant and anti-inflammatory properties which might contribute to neuro protective effects.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Carolina C Martins et al.
Progress in neuro-psychopharmacology & biological psychiatry, 98, 109803-109803 (2019-11-07)
The opioid withdrawal syndrome is defined as a complex phenomenon involving multiple cellular adaptations, which leads to the emergence of aversive physical and affective signs. The m-trifluoromethyl-diphenyl diselenide (m-CF3-PhSe)2 elicits an antidepressant-like effect by modulating the opioid system in different
Cleisson Schossler Garcia et al.
Molecular neurobiology, 58(10), 5078-5089 (2021-07-11)
Chronic pain and depression often coexist sharing common pathological mechanisms, and available analgesics and antidepressants have demonstrated limited clinical efficacy. Evidence has demonstrated that neuronal oxidative stress, apoptosis, and also glucocorticoid receptor dysregulation facilitate the occurrence and development of both
Contribution of Opioid and Nitrergic Systems to m-Trifluoromethyl diphenyl Diselenide Attenuates Morphine-Induced Tolerance in Mice
ACS Chemical Neuroscience, 13(7), 910-919 (2022)

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