Cas 104548-03-0,10-Benzyloxymethyl-2,5,8,11,14,17-hexaoxa-tricyclo[16.7.1.022,26]hexacosa-1(25),18(26),19,21,23-pentaene

104548-03-0

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Basic information

Product Name: 10-Benzyloxymethyl-2,5,8,11,14,17-hexaoxa-tricyclo[16.7.1.0^22,26]hexacosa-1⁽²⁵⁾,18⁽²⁶⁾,19,21,23-pentaene
Synonyms: 10-Benzyloxymethyl-2,5,8,11,14,17-hexaoxa-tricyclo[16.7.1.0^22,26]hexacosa-1⁽²⁵⁾,18⁽²⁶⁾,19,21,23-pentaene
CAS NO:104548-03-0
Molecular Formula:
Molecular Weight: 482.574
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: 10-Benzyloxymethyl-2,5,8,11,14,17-hexaoxa-tricyclo[16.7.1.0^22,26]hexacosa-1⁽²⁵⁾,18⁽²⁶⁾,19,21,23-pentaene(CAS DataBase Reference)
NIST Chemistry Reference: 10-Benzyloxymethyl-2,5,8,11,14,17-hexaoxa-tricyclo[16.7.1.0^22,26]hexacosa-1⁽²⁵⁾,18⁽²⁶⁾,19,21,23-pentaene(104548-03-0)
EPA Substance Registry System: 10-Benzyloxymethyl-2,5,8,11,14,17-hexaoxa-tricyclo[16.7.1.0^22,26]hexacosa-1⁽²⁵⁾,18⁽²⁶⁾,19,21,23-pentaene(104548-03-0)

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: 104548-03-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104548-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104548-03:
(8*1)+(7*0)+(6*4)+(5*5)+(4*4)+(3*8)+(2*0)+(1*3)=100
100 % 10 = 0
So 104548-03-0 is a valid CAS Registry Number.

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104548-03-0Relevant academic research and scientific papers

Cesium Fluoride Assisted Synthesis of Macrocyclic Polyethers with Aromatic Subunits

Czech, Bronislaw P.,Czech, Anna,Bartsch, Richard A.

, p. 1297 - 1300 (2007/10/02)

Several features of the synthesis of crown ethers with aromatic subunits by reactions of dihydroxyaromatic or bis(hydroxyaromatic) compounds with cesium fluoride and polyethylene glycol tosylates are explored.The method is utilized to prepare several new crown ethers and to synthesize known crown compounds in improved yields.

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