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2-methyl-4,4,4-triphenyl-1-butene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84803-39-4

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84803-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84803-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,0 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84803-39:
(7*8)+(6*4)+(5*8)+(4*0)+(3*3)+(2*3)+(1*9)=144
144 % 10 = 4
So 84803-39-4 is a valid CAS Registry Number.

84803-39-4Downstream Products

84803-39-4Relevant academic research and scientific papers

Synthesis, properties, and reactivity of palladium and nickel NHC complexes supported by combinations of allyl, cyclopentadienyl, and indenyl ligands

Bielinski, Elizabeth A.,Dai, Wei,Guard, Louise M.,Hazari, Nilay,Takase, Michael K.

, p. 4025 - 4037 (2013/09/02)

The synthesis of a series of Pd and Ni complexes containing combinations of 2-methylallyl (C4H7), cyclopentadienyl (C 5H5, Cp), and indenyl (C7H9, Ind) ligands is reported. In all cases these complexes are supported by the electron-donating N-heterocyclic carbene ligand 1,3-bis(2,6-diisopropylphenyl)- 1,3-dihydro-2H-imidazol-2-ylidene (IPr). The mixed Cp/2-methylallyl complexes (η1-Cp)(η3-2-methylallyl)Pd(IPr) ( CpAllPd) and (η5-Cp)(η1-2-methylallyl) Ni(IPr) (CpAllNi) were synthesized through the reaction of IPr with (Cp)(2-methylallyl)M (M = Ni, Pd). The binding mode of the ligands is different in the two complexes, and as a result the total valence electron count around the metal is 18 for the Ni complex and only 16 for the Pd species. In the case of Pd, an analogue of CpAllPd containing an indenyl ligand, (η1-Ind)(η3-2-methylallyl)Pd(IPr) ( IndAllPd), was synthesized through the reaction of (η3-Ind)Pd(IPr)Cl (IndClPd) with (2-methylallyl) magnesium chloride. The corresponding Ni complex (η5-Ind) (η1-2-methylallyl)Ni(IPr) (IndAllNi) could not be isolated. The binding modes of the ligands in the mixed indenyl/Cp complexes (η1-Ind)(η5-Cp)M(IPr) (M = Ni ( IndCpNi), Pd (IndCpPd)) were the same for both Ni and Pd. IndCpPd was prepared through the reaction of IndClPd with NaCp, while IndCpNi was synthesized through the reaction of (η5-Cp)Ni(IPr)Cl (CpClNi) with lithium indenyl. Similarly, the structures of the bis(Cp) complexes (η5-Cp) (η1-Cp)Ni(IPr) (CpCpNi) and (η5-Cp) (η1-Cp)Pd(IPr) (CpCpPd) were identical for the two different metals. In contrast to CpCpPd, which is an 18-electron complex, the related bis(indenyl) Pd complex (η3-Ind) (η1-Ind)Pd(IPr) (IndIndPd) is a 16-electron species, while no Ni analogue of IndIndPd was characterized. Preliminary reactivity studies with electrophiles indicate that, in all systems with mixed ligands, the η1-ligand is nucleophilic and reacts selectively. The complexes CpAllPd, CpAllNi, CpCpPd, CpCpNi, IndClPd, IndAllPd, and IndIndPd were characterized by X-ray crystallography.

Reactions of allylpalladium(II) complexes with free radicals

Reid,Freeman,Baird

, p. 1777 - 1778 (2007/10/03)

Allylpalladium(II) compounds react readily in benzene with free phenyl and trityl radicals, generated from the thermal decomposition of phenylazotriphenylmethane, and with free cyclohexyl radicals, generated from the photolysis of (cyclohexyl)(pyridine)cobaloxime; the reactions appear to involve initial attack of the radicals at palladium, followed by secondary processes which convert the coordinated allyl ligands preferentially to terminal rather than internal alkenes.

Scope and Limitations of Aliphatic Friedel-Crafts Alkylations. Lewis Acid Catalyzed Addition Reactions of Alkyl Chlorides to Carbon-Carbon Double Bonds

Mayr, Herbert,Striepe, Wilhelm

, p. 1159 - 1165 (2007/10/02)

Lewis acid catalyzed addition reactions of alkyl halides 1 with unsaturated hydrocarbons 2 have been studied. 1:1 addition products 3 are formed if the addends 1 dissociate faster than the corresponding products 3; otherwise, polymerization of 2 takes place.For reaction conditions under which 1 and 3 exist mainly undissociated, solvolysis constants of model compounds can be used to predict the outcome of any such addition reactions if systems with considerable steric hindrance are excluded.

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