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25,27-bis(2-(4-benzyloxyphenyl)ethoxy)-26,28-dihydroxy-p-tert-butylcalix[4]arene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 197796-03-5 Structure
  • Basic information

    1. Product Name: 25,27-bis(2-(4-benzyloxyphenyl)ethoxy)-26,28-dihydroxy-p-tert-butylcalix[4]arene
    2. Synonyms: 25,27-bis(2-(4-benzyloxyphenyl)ethoxy)-26,28-dihydroxy-p-tert-butylcalix[4]arene
    3. CAS NO:197796-03-5
    4. Molecular Formula:
    5. Molecular Weight: 1069.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 197796-03-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 25,27-bis(2-(4-benzyloxyphenyl)ethoxy)-26,28-dihydroxy-p-tert-butylcalix[4]arene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 25,27-bis(2-(4-benzyloxyphenyl)ethoxy)-26,28-dihydroxy-p-tert-butylcalix[4]arene(197796-03-5)
    11. EPA Substance Registry System: 25,27-bis(2-(4-benzyloxyphenyl)ethoxy)-26,28-dihydroxy-p-tert-butylcalix[4]arene(197796-03-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 197796-03-5(Hazardous Substances Data)

197796-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197796-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,7,9 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 197796-03:
(8*1)+(7*9)+(6*7)+(5*7)+(4*9)+(3*6)+(2*0)+(1*3)=205
205 % 10 = 5
So 197796-03-5 is a valid CAS Registry Number.

197796-03-5Relevant articles and documents

Head-to-Tail Connected Double Calix[4]arenes

Wasikiewicz,Rokicki,Kielkiewicz,Paulus,Boehmer

, p. 863 - 879 (1997)

New macrotricyclic compounds consisting of two calix[4]arene substructures connected by aliphatic chains of various length (three to five carbon atoms) between two opposite p-positions and two distal phenolic oxygens have been synthesized. Starting with p-tert-butyl-calix[4]arene, two O-protected phenolic units are attached via ether links in 1,3-position by reaction with the corresponding tosylates. After deprotection, the new calix[4]arene is formed by fragment condensation with 2,6-tobromomethylated 4-alkylphenols. The structure of one example (8c) has been confirmed by single crystal X-ray analysis. Both calixarene parts assume the cone conformation, a molecule of acetonitrile being included in both cavities.

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