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Home > Product > Precious Metal Catalyst > Palladium series catalysts > Palladium(II)(π-cinnamyl) Chloride Dimer

Palladium(II)(π-cinnamyl) Chloride Dimer

Catalog Number
ACM12131441
Product Name
Palladium(II)(π-cinnamyl) Chloride Dimer
Structure
CAS Number
12131-44-1
UN Number
UN 2811 6.1 / PGIII
MDL Number
MFCD16621470
IUPAC Name
palladium(2+);prop-2-enylbenzene;dichloride
Synonyms
Bis[cinnamyl palladium(II) chloride]
Category
organic noble metal
Molecular Weight
518.08
Exact Mass
507.82300
Molecular Formula
C18H18Cl2Pd2
Melting Point
218-220 °C
Purity
Pd >41.0%
Appearance
dark yellow powder
SMILES
C=C[CH-]C1=CC=CC=C1.C=C[CH-]C1=CC=CC=C1.[Cl-].[Cl-].[Pd+2].[Pd+2]
InChIKey
PHDNDSSMEIRHSI-UHFFFAOYSA-L
Symbol
GHS05, GHS06, GHS08
Safty Description
Danger
Hazard Statements
H315-H318-H331-H334
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1Synthesis of ([(11)C]carbonyl)raclopride and a comparison with ([(11)C]methyl)raclopride in a monkey PET study.

Rahman O1, Takano A2, Amini N2, Dahl K2, Kanegawa N2, Långström B3, Farde L2, Halldin C4.

Nucl Med Biol. 2015 Nov;42(11):893-8. doi: 10.1016/j.nucmedbio.2015.07.003. Epub 2015 Jul 15.

INTRODUCTION: The selective dopamine D2 receptor antagonist raclopride is usually labeled with carbon-11 using [(11)C]methyl iodide or [(11)C]methyl triflate for use in the quantification of dopamine D2 receptors in human brain. The aim of this work was to label raclopride at the carbonyl position using [(11)C]carbon monoxide chemistry and to compare ([(11)C]carbonyl)raclopride with ([(11)C]methyl)raclopride in non-human primate (NHP) using PET with regard to quantitative outcome measurement, metabolism of the labeled tracers and protein binding. Read More

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Tel:1-201-478-8534
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Address: 2200 Smithtown Avenue, Room 1 Ronkonkoma, NY 11779-7329 USA