Cas 204461-36-9,1-Benzyloxy-naphthalene-2-carboxylic acid 4-oxo-4H-3-oxa-dibenzo[c,g]phenanthren-2-yl ester

204461-36-9

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Basic information

Product Name: 1-Benzyloxy-naphthalene-2-carboxylic acid 4-oxo-4H-3-oxa-dibenzo[c,g]phenanthren-2-yl ester
Synonyms: 1-Benzyloxy-naphthalene-2-carboxylic acid 4-oxo-4H-3-oxa-dibenzo[c,g]phenanthren-2-yl ester
CAS NO:204461-36-9
Molecular Formula:
Molecular Weight: 572.617
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: 1-Benzyloxy-naphthalene-2-carboxylic acid 4-oxo-4H-3-oxa-dibenzo[c,g]phenanthren-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-Benzyloxy-naphthalene-2-carboxylic acid 4-oxo-4H-3-oxa-dibenzo[c,g]phenanthren-2-yl ester(204461-36-9)
EPA Substance Registry System: 1-Benzyloxy-naphthalene-2-carboxylic acid 4-oxo-4H-3-oxa-dibenzo[c,g]phenanthren-2-yl ester(204461-36-9)

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: 204461-36-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 204461-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,4,6 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 204461-36:
(8*2)+(7*0)+(6*4)+(5*4)+(4*6)+(3*1)+(2*3)+(1*6)=99
99 % 10 = 9
So 204461-36-9 is a valid CAS Registry Number.

204461-36-9Upstream product

204461-36-9Downstream Products

204461-36-9Relevant academic research and scientific papers

Synthesis and structure of a novel twofold lactone-bridged ternaphthyl

Bringmann, Gerhard,Wuzik, Andreas,Kraus, Juergen,Peters, Karl,Peters, Eva-M.

, p. 1545 - 1548 (1998)

The synthesis of the sterically distorted ternaphthyl-bislactone 4, by consecutive palladium-catalyzed coupling reactions of ester-type pre-fixed aryl segments, is described. The meso-form of this novel teraryl was found to be energetically favored as dem

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