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1,21,23,25-tetrapropyl-7,11,5,28-tetrakis(3-hydroxyphenoxymethyl)-2,20:13,19-methano-1H,21H,23H,25H-bis[1,3]dioxocino[5,4-i:5',4'-i']benzo[1,2-d:5,5-d']bis[1,3]benzodioxocine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

235107-75-2

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235107-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 235107-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,5,1,0 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 235107-75:
(8*2)+(7*3)+(6*5)+(5*1)+(4*0)+(3*7)+(2*7)+(1*5)=112
112 % 10 = 2
So 235107-75-2 is a valid CAS Registry Number.

235107-75-2Downstream Products

235107-75-2Relevant academic research and scientific papers

Facile synthesis and binding properties of C2ν container host based on resorcin[4]arene

Peak, Kyungsoo,Ihm, Chaesang,Ihm, Hyejae

, p. 4697 - 4700 (1999)

Two new C2ν container hosts were synthesized by capping of catechol- or resorcinol-fenced resorcin[4]arene with 1,2,4,5-tetrakis(bromomethyl)benzene and their Ka values were caculated directly from 1H NMR spectra. These hosts showed the binding properties for alkyl alcohols, methylene chloride, and tetrahydrofuran in CDCl3 or (CDCl2)2 at -40 deg C.

Molecular engineering. Part 5.1 Tuning the constrictive binding of container host by the atomic order of portal pillars

Ihm, Chaesang,Kim, Minkyu,Ihm, Hyejae,Paek, Kyungsoo

, p. 1569 - 1575 (2007/10/03)

Two D4h container hosts 12 and 13 with 4(CH2-O-bridge-O-CH2) portal pillars were obtained in good yields by stepwise synthetic routes and showed complementary complexation behaviors to their analogues with (O-CH2-bridge-CH2-O)4 portal pillars. 1H NMR spectral chemical shifts of host's inward-turned OCH2O protons were sensitive to guest change. The stability orders of hemicarceplexes were 12-p-(CH3CH2)2C6H4 > 12-p-(CH3O)2C6-H4 ? 12-o-(CH3O)2C6H4 > 12-m-(CH3O)2C6H4 and 13-CH3COCH2CH3 > 13-CH3COCH2CH(CH3)2 > 13-CH3-CON(CH3)2 > 13-CH3COOCH2CH3 > 13-CH3CH2CON(CH3)2 in terms of the activation energy barrier for decomplexation. Large solvent effects on the activation energy for decomplexation of hemicarceplexes were observed.

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