Cas 330186-50-0,5,11,17,23-tetra-tert-butyl-25-[(m-methylbenzyl)oxy]-26,27,28-trihydroxycalix[4]arene

330186-50-0

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Basic information

Product Name: 5,11,17,23-tetra-tert-butyl-25-[(m-methylbenzyl)oxy]-26,27,28-trihydroxycalix[4]arene
Synonyms: 5,11,17,23-tetra-tert-butyl-25-[(m-methylbenzyl)oxy]-26,27,28-trihydroxycalix[4]arene
CAS NO:330186-50-0
Molecular Formula:
Molecular Weight: 753.078
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5,11,17,23-tetra-tert-butyl-25-[(m-methylbenzyl)oxy]-26,27,28-trihydroxycalix[4]arene(CAS DataBase Reference)
NIST Chemistry Reference: 5,11,17,23-tetra-tert-butyl-25-[(m-methylbenzyl)oxy]-26,27,28-trihydroxycalix[4]arene(330186-50-0)
EPA Substance Registry System: 5,11,17,23-tetra-tert-butyl-25-[(m-methylbenzyl)oxy]-26,27,28-trihydroxycalix[4]arene(330186-50-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 330186-50-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 330186-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,1,8 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 330186-50:
(8*3)+(7*3)+(6*0)+(5*1)+(4*8)+(3*6)+(2*5)+(1*0)=110
110 % 10 = 0
So 330186-50-0 is a valid CAS Registry Number.

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330186-50-0Relevant academic research and scientific papers

Synthesis and Conformational Characteristics of Benzyl-Substituted p-tert-Butylcalixarenes

Alekseeva, E. A.,Mazepa, A. V.,Gren, A. I.

, p. 1786 - 1792 (2007/10/03)

(m-Methylbenzyloxy)-, bis(p-methylbenzyloxy)-, and bis(m-methylbenzyloxy)-p-tert-butylcalix[4]-arenes were prepared by reactions of p- and tert-butylcalix[4]arene with p- and m-methylbenzyl bromides in the presence of alkali metal carbonates. Silylation o

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