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3-<3-<3-(5-phenylsalicyl)-5-phenylsalicyl>-5-phenylsalicyl>-5-phenyl-2-hydroxybenzyl alcohol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81535-91-3

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81535-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81535-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,3 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81535-91:
(7*8)+(6*1)+(5*5)+(4*3)+(3*5)+(2*9)+(1*1)=133
133 % 10 = 3
So 81535-91-3 is a valid CAS Registry Number.

81535-91-3Relevant academic research and scientific papers

Calixarenes. 7. p-Phenycalixarene

Gutsche, C. David,No, Kwang Hyun

, p. 2708 - 2712 (2007/10/02)

p-Phenylcalixarene (11), in the cone conformation, is a basket-shaped compound containing a large cavity and, therefore, is of interest for studies of host-guest complexation.Its unequivocal synthesis has been achieved by the stepwise method of Hayes and Hunter, by starting with 2-bromo-4-phenylphenol and adding methylene and p-phenylphenol groups sequentially until a linear tetramer (9) is attained.Removal of the bromine followed by acid-catalyzed cyclization yields the calixarene 11, along with two other materials that are presumed to be the isomeric macrocyclic compounds 12 and 13. p-Phenylcalixarene synthesized in this fashion is different from the compound reported by Zinke from the condensation of p-phenylphenol and formaldehyde in the presence of base, and it appears that 11 is not a major product, and perhaps not even a minor product, of that reaction mixture.

Calixarenes. 8. Short, Stepwise Synthesis of p-Phenylcalixarene, p-Phenyl-p-tert-butylcalixarene, and Derived Products

No, Kwang Hyun,Gutsche, C. David

, p. 2713 - 2719 (2007/10/02)

Calixarenes (Schemes I-IV) have been previously obtained by a one-flask process (Zinke synthesis) and by a multistep process (Hayes and Hunter synthesis).The former has the advantage of speed and simplicity but the disadvantage of difficult-to-separate pr

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