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131298-22-1

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131298-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131298-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,9 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131298-22:
(8*1)+(7*3)+(6*1)+(5*2)+(4*9)+(3*8)+(2*2)+(1*2)=111
111 % 10 = 1
So 131298-22-1 is a valid CAS Registry Number.

131298-22-1Relevant articles and documents

Synthesis of 3-Methylthioindoles via Intramolecular Cyclization of 2-Alkynylanilines Mediated by DMSO/DMSO-d6 and SOCl2

Li, Xuemin,Zhang, Beibei,Zhang, Jingran,Wang, Xi,Zhang, Dongke,Du, Yunfei,Zhao, Kang

, p. 1211 - 1224 (2021/05/04)

The intramolecular cyclization of 2-alkynylanilines mediated by DMSO/SOCl2 was found to afford biologically interesting 3-methylthioindoles, which are rarely obtained by the exiting methods. DMSO could also be replaced with its deuterated count

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 (2016/07/23)

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

Quadri-synergetic effect for highly effective carbon dioxide fixation and its application to indoloquinolinone

Li, Suhua,Ma, Shengming

supporting information, p. 2387 - 2394,8 (2020/08/31)

The first copper-catalyzed cyclic anti-nucleometallation-carboxylation of 2-alkynylanilines with carbon dioxide in the presence of dimethylzinc (ZnMe 2) and cesium fluoride (CsF) for the effective synthesis of indolyl-3-carboxylic acids and indolodihydropyran-2-one is described. Through a mechanistic study, it is unveiled that the metal ions Cu2+, Zn 2+, Cs+ and F- are working together for this CO2-based highly efficient carboxylation. Copyright

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