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1345599-26-9

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1345599-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1345599-26-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,5,9 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1345599-26:
(9*1)+(8*3)+(7*4)+(6*5)+(5*5)+(4*9)+(3*9)+(2*2)+(1*6)=189
189 % 10 = 9
So 1345599-26-9 is a valid CAS Registry Number.

1345599-26-9Downstream Products

1345599-26-9Relevant articles and documents

Silica-supported tungstic acid (STA): A recyclable catalyst for the synthesis of 1H-indazolo [1,2-b]phthalazine-trione and spiro-triazolo[1,2-a]indazole-tetraone derivatives under solvent-free condition

Jadhav, Amol Maruti,Balwe, Sandip Gangadhar,Jeong, Yeon Tae

, p. 201 - 210 (2019/09/12)

An efficient one-pot synthesis of 1 H-indazolo[1,2-b]phthalazine-trione and spiro-triazolo[1,2-a]indazole-tetraone derivatives via three-component condensation reaction of phthalhydrazide or 4-phenylurazole, aldehydes or isatins and dimedone in the presen

Preparation, characterization, and use of novel Cu@Fe3O4 MNPs in the synthesis of tetrahydrobenzimidazo[2,1-b] quinazolin-1(2 H)-ones and 2 H -indazolo[2,1- b] phthalazine-triones under solvent-free conditions

Jiang, Lilin,Druzhinin, Zumrat

, p. 15061 - 15072 (2019/05/24)

Cu@Fe3O4 MNPs as novel nanomagnetic reagents were prepared to investigate their catalytic behavior in the preparation of tetrahydrobenzimidazo[2,1-b]quinazolin-1(2H)-ones, as important biologically active compounds. Then, characteriz

Pentaerythritol as efficient H-bonding organocatalyst for synthesis of indazolo[2,1-b]phthalazine-trione derivatives

Farahmand, Shohreh,Ayazi-Nasrabadi, Roya,Mokhlesi, Mohammad,Zolfigol, Mohammad Ali

, p. 3795 - 3807 (2019/04/17)

Pentaerythritol was applied as an effective, biodegradable, nontoxic, mild, and commercially available H-bonding organocatalyst for synthesis of indazolo[2,1-b]phthalazine-trione derivatives via one-pot three-component condensation of aromatic aldehydes,

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