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5,6-dimethyl-2-phenylisoindoline-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135950-48-0

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135950-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135950-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,5 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135950-48:
(8*1)+(7*3)+(6*5)+(5*9)+(4*5)+(3*0)+(2*4)+(1*8)=140
140 % 10 = 0
So 135950-48-0 is a valid CAS Registry Number.

135950-48-0Downstream Products

135950-48-0Relevant academic research and scientific papers

Palladium on carbon: An efficient, heterogeneous and reusable catalytic system for carbonylative synthesis of N-substituted phthalimides

Khedkar, Mayur V.,Khan, Shoeb R.,Sawant, Dinesh N.,Bagal, Dattatraya B.,Bhanage, Bhalchandra M.

, p. 3415 - 3422 (2011)

The application of palladium on carbon (Pd/C) as a heterogeneous recyclable catalyst was investigated for the double carbonylation of o-dihaloarenes with amines providing excellent yield of N-substituted phthalimides in shorter reaction time as compared to earlier reported homogeneous protocols. Furthermore, the scope of the developed protocol was applied for the synthesis N-substituted phthalimides from o-halobenzoates and o-halobenzoic acid via a single step carbonylative cyclization reaction. The developed methodology describes an efficient one-step approach for the synthesis of an important class of heterocycles and tolerates a wide variety of functional groups. It circumvents the use of phosphine ligands with an additional advantage of catalyst recyclability for up to eight consecutive cycles. Copyright

Ruthenium(II)-catalyzed N-substituted phthalimide synthesis via C-H activation/[3+2] annulation

Dong, Xue-Fen,Fan, Juan,Shi, Xian-Ying,Liu, Ke-Yan,Wang, Peng-Min,Wei, Jun-Fa

, p. 55 - 61 (2015/02/18)

Ruthenium-catalyzed intermolecular [3 + 2] annulation pathway for aromatic acids with isocyanates to afford N-substituted phthalimide in one step is demonstrated, which provides an efficient process to direct preparation of phthalimide from commercially a

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