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Pd[κ1-C,κ1-N-C=(C6H5)C(Cl)CH2N(CH3)2](Cl)(pyridine) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

643752-04-9

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643752-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 643752-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,3,7,5 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 643752-04:
(8*6)+(7*4)+(6*3)+(5*7)+(4*5)+(3*2)+(2*0)+(1*4)=159
159 % 10 = 9
So 643752-04-9 is a valid CAS Registry Number.

643752-04-9Downstream Products

643752-04-9Relevant academic research and scientific papers

Atropisomerism in palladacycles derived from the chloropalladation of heterosubstituted alkynes

Zanini, Mara L.,Meneghetti, Mario R.,Ebeling, Günter,Livotto, Paolo R.,Rominger, Frank,Dupont, Jairton

, p. 527 - 536 (2008/10/08)

The chloropalladation of 2-substituted phenyl N,N-propargylamines, Y-2-C6H4C≡CCH2NMe2 (1a, Y=H; 2a, Y=CF3; 3a, Y=OMe; 4a, Y=SMe and 5a, Y=NH2) affords palladacycles in different ratios of isomers (geometric and atropisomers). In solution, the parent alkyne (Y=H) and the CF3 substituted derivative generate a mixture of cisoid and transoid chloro-bridged dimer palladacycles of the type {Pd[κ1-C, κ1-N-C=(Y-2-C 6H4)C(Cl)CH2NMe2](μ-Cl)} 2. Moreover, in the case of Y=CF3 palladacyclic derivative each of the geometric isomers comprises a mixture of two diastereoisomers due to the restricted rotation of the C(vinyl)-C(aryl) sigma bond (atropisomers). Palladacycles 1a (Y=H) and 2a (Y=CF3) crystallize as the single transoid and cisoid-anti isomer, respectively. The OMe substituted alkyne yields a similar dimeric compound that crystallizes as a single cisoid-anti isomer. In solution this dimeric compound is in fast equilibrium with a monomeric pincer compound of the type Pd[κ 1-C, κ1-N, κ1-O-C=(MeO-2-C 6H4)C(Cl)CH2NMe2](Cl) assisted through the weak coordination of the OMe group. Pincer palladacycles Pd[κ1-C, κ1-N, κ1-Y-C=(Y-2- C6H4)C(Cl)CH2NMe2](Cl) (Y=SMe and NH2) were the sole products obtained in the chloropalladation of alkynes 4a and 5a. The bridge splitting reaction of the dimeric palladacycles 1b-3b with pyridine is highly selective, affording exclusively the corresponding monomeric compounds 1c-3c. The monomeric palladacycle 2d, which comprises a mixture of two atropisomers (2:1 ratio of anti/syn) was obtained from the reaction of 2b with 2-methylpyridine. Theoretical calculations indicated that the anti isomer of 2d is 5.42 kJmol-1 more stable than its syn isomer.

The retro-chloropalladation reaction of heterosubstituted alkynes

Zanini, Mara L.,Meneghetti, Mario R.,Ebeling, Gunter,Livotto, Paolo R.,Rominger, Frank,Dupont, Jairton

, p. 1665 - 1671 (2008/10/08)

The bridge-splitting reaction of dimeric palladacycles of the type {Pd[κ1-C, κ1-N-C(R) = C(Cl)CH2NMe2](μ-Cl)}2 (R = Ph, Me, CH2CH2OH), derived from the chloropalladation of propa

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