Cas 1318073-59-4,2-(p-bromobenzyl)-5,11,17,23-tetra-tert-butyl-14-ethyl-25,26,27,28-tetramethoxycalix[4]arene

1318073-59-4

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Basic information

Product Name: 2-(p-bromobenzyl)-5,11,17,23-tetra-tert-butyl-14-ethyl-25,26,27,28-tetramethoxycalix[4]arene
Synonyms: 2-(p-bromobenzyl)-5,11,17,23-tetra-tert-butyl-14-ethyl-25,26,27,28-tetramethoxycalix[4]arene
CAS NO:1318073-59-4
Molecular Formula:
Molecular Weight: 902.108
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: 2-(p-bromobenzyl)-5,11,17,23-tetra-tert-butyl-14-ethyl-25,26,27,28-tetramethoxycalix[4]arene(CAS DataBase Reference)
NIST Chemistry Reference: 2-(p-bromobenzyl)-5,11,17,23-tetra-tert-butyl-14-ethyl-25,26,27,28-tetramethoxycalix[4]arene(1318073-59-4)
EPA Substance Registry System: 2-(p-bromobenzyl)-5,11,17,23-tetra-tert-butyl-14-ethyl-25,26,27,28-tetramethoxycalix[4]arene(1318073-59-4)

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: 1318073-59-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1318073-59-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,8,0,7 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1318073-59:
(9*1)+(8*3)+(7*1)+(6*8)+(5*0)+(4*7)+(3*3)+(2*5)+(1*9)=144
144 % 10 = 4
So 1318073-59-4 is a valid CAS Registry Number.

1318073-59-4Upstream product

589-15-1 1-bromomethyl-4-bromobenzene

1318073-59-4Downstream Products

1318073-59-4Relevant academic research and scientific papers

Bridge-disubstituted calix[4]arenes obtained via a new preparative route. Synthesis and structural study

Fischer, Conrad,Lin, Guisheng,Seichter, Wilhelm,Weber, Edwin

, p. 5656 - 5662 (2011)

A series of calix[4]arenes bearing various substituents including alkyl, p-bromobenzyl, carboxy and allyl at opposite methylene bridges has been synthesized via successive metallation followed by nucleophilic substitution. In a first step, mono-lithiated

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