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2-[2-(2-amino-5-chlorophenyl)ethynyl]-4-chloroaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1224955-25-2

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1224955-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1224955-25-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,9,5 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1224955-25:
(9*1)+(8*2)+(7*2)+(6*4)+(5*9)+(4*5)+(3*5)+(2*2)+(1*5)=152
152 % 10 = 2
So 1224955-25-2 is a valid CAS Registry Number.

1224955-25-2Downstream Products

1224955-25-2Relevant academic research and scientific papers

Cu(OAc)2-Mediated Cascade Annulation of Diarylalkyne Sulfonamides through Dual C-N Bond Formation: Synthesis of 5,10-Dihydroindolo[3,2-b]indoles

Yu, Junchao,Zhang-Negrerie, Daisy,Du, Yunfei

, p. 3322 - 3325 (2016)

An unusual cascade reaction featuring annulation of diarylalkyne sulfonamides to form 5,10-dihydroindolo[3,2-b]indoles has been realized with Cu(OAc)2 as the sole oxidant. This unprecedented process encompasses two sequential C-N bond formation

Pt(IV)-catalyzed hydroamination triggered cyclization: A strategy to fused pyrrolo[1,2- a ]quinoxalines, Indolo[1,2- a ]quinoxalines, and Indolo[3,2- c ]quinolines

Patil, Nitin T.,Kavthe, Rahul D.,Shinde, Valmik S.,Sridhar, Balasubramanian

supporting information; experimental part, p. 3371 - 3380 (2010/07/02)

A PtCl4-catalyzed hydroamination-triggered cyclization strategy to access biologically interesting N-containing heterocycles such as pyrrolo[1,2-a]quinoxalines, indolo[1,2-a]quinoxalines, and indolo[3,2-c] quinolines is described. The reaction makes use of aminoaromatics such as 1-(2-aminophenyl)pyrroles, N-(2-aminophenyl)indoles, 2-(2-aminophenyl)indoles, and alkynes having a tethered hydroxyl group. Mechanistically, the reaction is very appealing since it involves multiple catalytic cycles catalyzed by a single metal catalyst PtCl4. We observed a remarkable enhancement of the rate when reactions were run under microwave-assisted conditions.

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