Cas 1394124-90-3,diethyl 1-(6-(benzyloxy)benzo[d][1,3]dioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphthalene-2,3-dicarboxylate

1394124-90-3

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Basic information

Product Name: diethyl 1-(6-(benzyloxy)benzo[d][1,3]dioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphthalene-2,3-dicarboxylate
Synonyms: diethyl 1-(6-(benzyloxy)benzo[d][1,3]dioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphthalene-2,3-dicarboxylate
CAS NO:1394124-90-3
Molecular Formula:
Molecular Weight: 574.584
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: diethyl 1-(6-(benzyloxy)benzo[d][1,3]dioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphthalene-2,3-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl 1-(6-(benzyloxy)benzo[d][1,3]dioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphthalene-2,3-dicarboxylate(1394124-90-3)
EPA Substance Registry System: diethyl 1-(6-(benzyloxy)benzo[d][1,3]dioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphthalene-2,3-dicarboxylate(1394124-90-3)

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: 1394124-90-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1394124-90-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,1,2 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1394124-90:
(9*1)+(8*3)+(7*9)+(6*4)+(5*1)+(4*2)+(3*4)+(2*9)+(1*0)=163
163 % 10 = 3
So 1394124-90-3 is a valid CAS Registry Number.

1394124-90-3Upstream product

1394124-90-3Downstream Products

1394124-90-3Relevant academic research and scientific papers

Total synthesis of 60-hydroxyjusticidin A

Xiong, Lu,Bi, Ming-Gang,Wu, Song,Tong, Yuan-Feng

, p. 322 - 326 (2012)

The first total synthesis of 6′-hydroxyjusticidin A, isolated from Justicia procumbens L. with good inhibitory activity against cancer cells, has been accomplished. The structure was confirmed by 1H NMR, 13C NMR, and HR-ESI-MS. The key steps involved a Diels-Alder cycloaddition reaction and a reduction in NaBH4.

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