C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2⁽¹⁺⁾*Cl^(1-) = C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2Cl

Base Information

Chemical Name:C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2⁽¹⁺⁾*Cl^(1-) = C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2Cl
CAS No.:102808-70-8
Molecular Formula:C₁₆H₂₄N₃Pd*Cl
Molecular Weight:400.26
Hs Code.:

C<sub>10</sub>H<sub>6</sub>CH(CH<sub>3</sub>)N(CH<sub>3</sub>)2Pd(NH<sub>2</sub>CH<sub>2</sub>)2<sup>(1+)</sup>*Cl<sup>(1-)</sup> = C<sub>10</sub>H<sub>6</sub>CH(CH<sub>3</sub>)N(CH<sub>3</sub>)2Pd(NH<sub>2</sub>CH<sub>2</sub>)2Cl

Synonyms:C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2⁽¹⁺⁾*Cl^(1-) = C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2Cl

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Chemical Property of C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2⁽¹⁺⁾*Cl^(1-) = C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2Cl

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Technology Process of C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2⁽¹⁺⁾*Cl^(1-) = C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2Cl

There total 3 articles about C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2⁽¹⁺⁾*Cl^(1-) = C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2Cl which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 94.0%

: (C₁₀H₆CH(CH₃)N(CH₃)2)2Pd₂(Cl)(As(CH₃)(C₆H₄CH₂OCH₃)CH₂CH₂S)

: 102808-70-8
C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2⁽¹⁺⁾*Cl^(1-) = C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2Cl

: {SP-4,3-{(S),(R)}}-{dimethyl(1-(2-naphthyl)ethyl)aminato-C⁽²⁾,N}{(methyl(2-(methoxymethyl)phenyl)arsino)ethanethiolato-As,S}palladium(II)

Guidance literature:: In water; a soln. of (S(As),S(S),R,R)-Pd-compd. was stirred for 1 h in contact with a soln. of 1,2-ethanediamine in H2O, the organic layer was then separated and dried (MgSO4), removal of the solvent afforded a yellow glass that could not be induced to cryst.;; elem. anal.; the aq. layer contained the ionic Pd chloride complex;;
DOI:10.1021/ja00248a030

Reference yield: 88.0%

: 102916-61-0
[Pd₂Cl(C₁₀H₆CH(CH₃)N(CH₃)2)2(SC₂H₄As(CH₃)C₆H₅)]*0.67CH₂Cl₂

: 107-15-3,85404-18-8
ethylenediamine

: 102808-70-8
C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2⁽¹⁺⁾*Cl^(1-) = C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2Cl

: 102808-69-5
[SP-4-3-[S-(R(*),S(*))]]-[dimethyl(1-(α-naphthyl)ethyl)aminato-C(2),N][2-(methylphenylarsino)ethanethiolato]palladium(II)

Guidance literature:: In dichloromethane; water; stirring vor 1 h; sepn. of the org. phase, washing with water, drying over MgSO4, dissolving in CH2Cl2 and concn.; elem. anal.;

Reference yield: 87.0%

: 139493-23-5
chlorobis{(R)-1{1-(dimethylamino)ethyl}-2-naphthalenyl-C,N}{μ-{(S)-2-(methylphenylphosphino)ethanethiolato-P,S}dipalladium(II)}-dichloromethane

: 139461-42-0
{SP-4-4-1(R),4(S)}-{1-{1-(dimethylamino)ethyl}-2-naphthalenyl-C,N}{2-(methylphenylphosphino)ethanethiolato-P,S}palladium(II)

: 102808-70-8
C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2⁽¹⁺⁾*Cl^(1-) = C₁₀H₆CH(CH₃)N(CH₃)2Pd(NH₂CH₂)2Cl

Guidance literature:: With diamino-1,2-ethane; In dichloromethane; water; Pd-compound in CH2Cl2 treated with H2NCH2CH2NH2 in H2O, stirred for 1 h (Ar); org. from aq. phases sepd., content of org. phase recrystd. (dichloromethane-methanol mixt.); elem. anal.; aq. phase concd.;