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toluene-4-sulfonic acid 2-decyl-1-tetradecyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132004-78-5

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132004-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132004-78-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,0 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132004-78:
(8*1)+(7*3)+(6*2)+(5*0)+(4*0)+(3*4)+(2*7)+(1*8)=75
75 % 10 = 5
So 132004-78-5 is a valid CAS Registry Number.

132004-78-5Relevant academic research and scientific papers

Separation of lanthanides and actinides(III) using tridentate benzimidazole, benzoxazole and benzothiazole ligands

Drew, Michael G. B.,Hill, Clement,Hudson, Michael J.,Iveson, Peter B.,Madic, Charles,Vaillant, Ludovic,Youngs, Tristan G. A.

, p. 462 - 470 (2004)

The ability of new hydrophobic tridentate ligands based on 2,6-bis(benzimidazol-2-yl)pyridine, 2,6-bis(benzoxazol-2-yl)pyridine and 2,6-bis(benzothiazol-2-yl)pyridine to selectively extract americium(III) from europium(III) was measured. The most promisin

Synthesis of thienopyrrolodione-based copolymers and their application in organic thin-film transistors

Lee, Ji Eun,Kim, Yebyeol,Ha, Jong-Jin,An, Tae Kyu,Kim, Yun-Hi

, p. 5662 - 5668 (2017/05/08)

Two thienopyrrolodione (TPD)-based polymers, 24DTT-TPD and 24DTS-TPD, were synthesized by carrying out Stille coupling reactions. The obtained polymers were characterized by 1H NMR, FT-IR, mass analysis, UV-visible spectroscopy, cyclic voltammetry, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The deposited films were characterized by X-ray diffraction. Synthesized polymers showed good solubility in common solvents. The solution-processed organic field-effect transistors showed field-effect mobility values of 4.5 × 10-5 cm2/Vs for 24DTT-TPD and 2.9 × 10-2 cm2/Vs for 24 DTS-TPD at optimal conditions.

Method for synthesis of peptide using a carrier

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Page/Page column 24, (2016/04/05)

Disclosed are a carrier for use for separation purpose and a method for separation of a compound which enable a chemical reaction to be performed in a liquid phase, enable a compound of interest to be separated from the liquid phase after the completion of the reaction readily, enable the separated compound to be evaluated by structural analysis or the like while the compound being bound to the carrier, and enable the compound to be separated from the carrier readily. A carrier for separation which has a reaction site capable of reacting with other compound on a benzene ring, and a long-chain group having a specified carbon atom(s) at each of the ortho-position and the para-position of the reaction site through an oxygen atom.

A bundled-stack discotic columnar liquid crystalline phase with inter-stack electronic coupling

Wang,Sun,Günba,Zhang,Grozema,Xiao,Jin

supporting information, p. 11837 - 11840 (2015/07/15)

The first compound capable of forming a bundled-stack discotic columnar liquid crystalline (BSDCLC) phase was designed and synthesized. The unique perylene anhydride inter-stack interaction was found to be the key to the formation of the BSDCLC structure

Photochromism of a water-soluble vesicular [2.2]paracyclophane-bridged imidazole dimer

Mutoh, Katsuya,Abe, Jiro

supporting information; experimental part, p. 8868 - 8870 (2011/10/01)

Here we report the first photochromism of a newly designed [2.2]paracyclophane-bridged imidazole dimer in water. The photochromic dye with a hydrophilic and a hydrophobic substituent forms vesicles in water and shows instantaneous colouration upon UV ligh

CARRIER FOR SEPARATION, METHOD FOR SEPARATION OF COMPOUND, AND METHOD FOR SYNTHESIS OF PEPTIDE USING THE CARRIER

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Page/Page column 30-31, (2010/11/26)

Disclosed are a carrier for use for separation purpose and a method for separation of a compound which enable a chemical reaction to be performed in a liquid phase, enable a compound of interest to be separated from the liquid phase after the completion o

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