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Acetic acid 4-[5-(4-acetoxy-benzylsulfanyl)-4',5'-bis-methylsulfanyl-[2,2']bi[[1,3]dithiolylidene]-4-ylsulfanylmethyl]-phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144868-63-3

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144868-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144868-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,6 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144868-63:
(8*1)+(7*4)+(6*4)+(5*8)+(4*6)+(3*8)+(2*6)+(1*3)=163
163 % 10 = 3
So 144868-63-3 is a valid CAS Registry Number.

144868-63-3Downstream Products

144868-63-3Relevant academic research and scientific papers

Methylthio Substituted 2,5-Bis(1',3'-dithiol-2'-ylidene)-1,3,4,6-tetrathiapentalene. A Bis-Fused Tetrathiafulvalene

Misaki, Yohji,Nishikawa, Hiroyuki,Kawakami, Kazuya,Koyanagi, Shiro,Yamabe, Tokio,Shiro, Motoo

, p. 2321 - 2324 (1992)

Synthesis of the title compound (1), and its molecular structure determined by X-ray crystallographic analysis, and electrochemical property investigated by cyclic voltammetry are described.Several cation radical salts of 1 have been prepared by electroch

Synthesis of Unsymmetrical Tetrakis(alkylsulfanyl)tetrathiafulvalene Derivatives

Gemmell, Colin,Janairo, Gerardo C.,Kilburn, Jeremy D.,Ueck, Henning,Underhill, Allan E.

, p. 2715 - 2720 (2007/10/02)

The p-acetoxybenzylsulfanyl protecting group is compatible with the triethylphosphite mediated cross-coupling of 4,5-bis(alkylsulfanyl)-1,3-dithiol-2-ones, providing access to bis(protected)tetrathiafulvalenes, and thus to tetrathiafulvalenedithiolate dia

A straightforward approach to the synthesis of unsymmetrical tetrathioalkyl tetrathiafulvalene derivatives

Gemmell,Kilburn,Ueck,Underhill

, p. 3923 - 3926 (2007/10/02)

The p-acetoxybenzylthio protecting group has been found to be compatible with the triethylphosphite mediated cross-coupling of 4,5-dialkylthio-1,3-dithiol-2-ones, providing access to the tetrathiolate 5, and to dithiolates 11a and 11b, which are excellent

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