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1134205-15-4

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1134205-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1134205-15-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,4,2,0 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1134205-15:
(9*1)+(8*1)+(7*3)+(6*4)+(5*2)+(4*0)+(3*5)+(2*1)+(1*5)=94
94 % 10 = 4
So 1134205-15-4 is a valid CAS Registry Number.

1134205-15-4Relevant articles and documents

Cu(I)–N-heterocyclic carbene-catalyzed base free C–N bond formation of arylboronic acids with amines and azoles

Zhang, Maoyuan,Xu, Zengbing,Shi, Dabin

, (2021)

A new N-heterocyclic carbene (NHC) precursor of imidazolium chloride and its corresponding Cu(I)–NHC complex 1 was synthesized. The complex 1 was found to be a highly effective catalyst for Chan-Evans-Lam coupling of arylboronic acid with amines and azoles (including imidazole, pyrazole and triazole), without addition of base at room temperature. Various substituents on three substrates can be tolerated, giving the desired coupling products in good to excellent yields (62–94%). The method is practical and offers an alternative to the corresponding copper-catalyzed Chan-Evans-Lam process for the construction of C–N bonds.

CATALYSTS FOR POLYMERIZING CYCLIC OLEFIN

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Page/Page column 34, (2010/11/26)

Provided is a metal catalyst complex for preparing a cyclic olefin-based polymer by addition polymerization of a cyclic olefin-based monomer, which is represented by Formula 1 below: [M(L1)x (L'2)y(L3)z]a[Ani]b wherein M is a Group X metal; [M(L1)x (L'2)y(L3)z] is a cationic precatalyst; L1 is an anionic hydrocarbyl-containing ligand; L'2 is a neutral ligand; L3 is an N-heterocyclic carbene ligand; [Ani] is an anion capable of weakly coordinating with the metal M; x is 1 or 2; y is 0 to 4; z is 1 or 2; 2≤x+y+z≤6; a and b are each 1 to 10. The metal catalyst complex has an N-heterocyclic carbene ligand, and thus, is excellent in thermal stability and reactivity.

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