Cas 790676-04-9,5,17-bis(4-methylbenzamido)-11,23-dinitro-25,26,27,28-tetrakis(pentyloxy)calix[4]arene

790676-04-9

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Basic information

Product Name: 5,17-bis(4-methylbenzamido)-11,23-dinitro-25,26,27,28-tetrakis(pentyloxy)calix[4]arene
Synonyms: 5,17-bis(4-methylbenzamido)-11,23-dinitro-25,26,27,28-tetrakis(pentyloxy)calix[4]arene
CAS NO:790676-04-9
Molecular Formula:
Molecular Weight: 1061.33
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: 5,17-bis(4-methylbenzamido)-11,23-dinitro-25,26,27,28-tetrakis(pentyloxy)calix[4]arene(CAS DataBase Reference)
NIST Chemistry Reference: 5,17-bis(4-methylbenzamido)-11,23-dinitro-25,26,27,28-tetrakis(pentyloxy)calix[4]arene(790676-04-9)
EPA Substance Registry System: 5,17-bis(4-methylbenzamido)-11,23-dinitro-25,26,27,28-tetrakis(pentyloxy)calix[4]arene(790676-04-9)

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: 790676-04-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 790676-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,6,7 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 790676-04:
(8*7)+(7*9)+(6*0)+(5*6)+(4*7)+(3*6)+(2*0)+(1*4)=199
199 % 10 = 9
So 790676-04-9 is a valid CAS Registry Number.

790676-04-9Upstream product

790676-04-9Downstream Products

790676-04-9Relevant academic research and scientific papers

Selective derivatization of calix[4]arenes via amino groups attached to the wide rim

Bogdan, Anca,Vysotsky, Myroslav O.,Boehmer, Volker

, p. 1009 - 1026 (2004)

A new strategy is proposed for the synthesis of tetraether derivatives of calix[4]arenes bearing at the wide rim nitro and phthalimido groups in well defined positions. Since both groups are precursors of amino functions, calix[4]arenes substituted by dif

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