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p-phenylcalix[5]arene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

853918-67-9

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853918-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 853918-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,9,1 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 853918-67:
(8*8)+(7*5)+(6*3)+(5*9)+(4*1)+(3*8)+(2*6)+(1*7)=209
209 % 10 = 9
So 853918-67-9 is a valid CAS Registry Number.

853918-67-9Downstream Products

853918-67-9Relevant academic research and scientific papers

Direct synthesis of deep cavity p-Phenylcalix [4] arene in poly(ethylene glycol), and its self-association in the solid state

Makha, Mohamed,Raston, Colin L.,Sobolev, Alexandre N.

, p. 260 - 262 (2006)

p-Phenylcalix[4]arene is formed directly fromp-phenylphenol in 66% yield (50% isolated yield) using poly(ethylene glycol) as the reaction medium, with crystallization of the pure cavitand from toluene mediated by p-earborane. The solid-state structure comprises interlocking columnar arrays. CSIRO 2006.

Inter-digitation approach to encapsulation of C60: [C60 ? (p-phenylcalix[5]arene)2]

Makha, Mohamed,Hardie, Michaele J.,Raston, Colin L.

, p. 1446 - 1447 (2007/10/03)

p-Phenylcalix[5]arene shows a strong and selective binding of C60 in toluene resulting in crystallisation of a hemispherically inter-digitated 2:1 complex; the receptor itself crystallises from toluene with self assembly through phenyl group inclusion.

Direct synthesis of calixarenes with extended arms: p-phenylcalix[4,5,6,8]arenes and their water-soluble sulfonated derivatives

Makha, Mohamed,Raston, Colin L

, p. 6215 - 6217 (2007/10/03)

p-Phenylcalix[4,5,6,8]arenes have been isolated from the base catalysed condensation of p-phenylphenol with formaldehyde in tetralin, and selectively converted to the corresponding sulfonated derivatives using sulfuric or chlorosulfonic acids.

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