| Identification | Back Directory | [Name]
PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II) | [CAS]
884879-23-6 | [Synonyms]
GJB3
CX 31
Umicore CX31
Gap junction beta-3 protein
UMicore CX31, 16% Pd, Product of UMicore
ANTI-CONNEXIN 31(C-TERMINAL) antibody produced in rabbit
PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II)
(1,3-Bis(2,6-diisopropylphenyl)-1H-imidazol-2(3H)-ylidene)chloro(cinnamyl)palladate(II)
[1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloro[3-phenylallyl]palladium(II) 95%
Chloro[(1,2,3-η)-3-phenyl-2-propenyl][1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene]palladium(II)
Chloro[(1,2,3-η)-3-phenyl-2-propenyl][1,3-bis(2,6-di-i-propylphenyl)iMidazol-2-ylidene]palladiuM(II),97%
Chloro[(1,2,3-)-3-phenyl-2-propenyl][1,3-bis(2,6-di-i-propylphenyl)iMidazol-2-ylidene]palladiuM(II),Min.97%
Chloro[(1,2,3-n)-3-phenyl-2-propenyl][1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene]palladium(II), min. 97%
Chloro[(1,2,3-η)-3-phenyl-2-propenyl][1,3-bis(2,6-di-i-propylphenyl) imidazol-2-ylidene]palladium(II), min. 97%
Chloro[(1,2,3-n)-3-phenyl-2-propenyl][1,3-bis(2,6-di-i-propylphenyl)imidazol-
2-ylidene]palladium(II), min. 97%
Palladium, [1,3-bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-2H-imidazol-2-ylidene]chloro[(1,2,3-η)-1-phenyl-2-propen-1-yl]-, stereoisomer | [Molecular Formula]
Neolyst CX31 | [MDL Number]
MFCD11045095 | [MOL File]
884879-23-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
205-208°C | [storage temp. ]
-20°C | [form ]
powder | [Appearance]
Light yellow to yellow Solid | [InChIKey]
RWGNZUQSYXTZIX-UHFFFAOYSA-M | [SMILES]
N1(C(N(C=C1)C1C(C(C)C)=CC=CC=1C(C)C)=[Pd]Cl)C1=C(C(C)C)C=CC=C1C(C)C.[CH]([CH]C1=CC=CC=C1)[CH2] |^1:31,32,39| |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow crystal | [Uses]
Catalyst for Suzuki coupling (eq. 1) Catalyst for Buchwald-Hartwig amination reaction (eq. 2). | [reaction suitability]
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst | [Safety Profile]
S22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37 - Wear suitable protective clothing and gloves. |
| Questions And Answer | Back Directory | [Reactions]
- Catalyst used for room temperature Suzuki-Miyaura couplings.
- Catalyst used for rapid, room temperature Buchwald-Hartwig and Suzuki-Miyaura coupling reactions.
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J & K SCIENTIFIC LTD.
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T&W GROUP
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Sigma-Aldrich
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