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3,4-DIIODO-2,5-DIMETHYLTHIOPHENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40197-05-5

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40197-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40197-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,9 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40197-05:
(7*4)+(6*0)+(5*1)+(4*9)+(3*7)+(2*0)+(1*5)=95
95 % 10 = 5
So 40197-05-5 is a valid CAS Registry Number.

40197-05-5Relevant academic research and scientific papers

Metallic catalysts for chemo-, regio-and stereoselective reactions, and corresponding precursors

-

, (2008/06/13)

Metallic catalysts of the general formula (I) and their precursors, suitable for chemo- regio- and stereoselective reactions, derived from ortho-bis-(1-phospholanyl)-heteroarenes. The new catalysts are characterized by the presence of two homomorphic phospholanic rings set in adjacent positions of an aromatic pentatomic heterocycle.

Synthesis of annulated dioxins as electron-rich donors for cation radical salts

Hellberg, Jonas,Dahlstedt, Emma,Pelcman, Margit E.

, p. 8899 - 8912 (2007/10/03)

The synthesis of a series of new alkoxylated linearly annulated dioxins is described together with their cyclic voltammetric behavior and some preliminary result on their ability to form cation radical salts. Of these dioxins, seven (8, 12, 19, 21, 27, 33, 34) are the first representatives of entirely new heterocyclic systems. Dioxins 8, 21, 22 and 27 gave good quality cation radical salts upon electrocrystallization. Graphical Abstract

Halogenation Using Quaternary Ammonium Polyhalides. XXXI. Halogenation of Thiophene Derivatives with Benzyltrimethylammonium Polyhalides

Okamoto, Tsuyoshi,Kakinami, Takaaki,Fujimoto, Hiroshi,Kajigaeshi, Shoji

, p. 2566 - 2568 (2007/10/02)

The reactions of thiophene derivatives with benzyltrimethylammonium tetrachloroiodate, benzyltrimethylammonium tribromide, and benzyltrimethylammonium dichloroiodate in acetic acid or in acetic acid-zinc chloride under mild conditions gave chloro-, bromo-, and iodo-substituted thiophene derivatives, respectively, in satifactory yields.

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