Cas 693219-96-4,1-{6-[2,3,4-trimethoxy-6-(2-methoxy-ethoxymethoxymethyl)-phenyl]-benzo[1,3]dioxol-5-yl}-ethanol

693219-96-4

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Basic information

Product Name: 1-{6-[2,3,4-trimethoxy-6-(2-methoxy-ethoxymethoxymethyl)-phenyl]-benzo[1,3]dioxol-5-yl}-ethanol
Synonyms: 1-{6-[2,3,4-trimethoxy-6-(2-methoxy-ethoxymethoxymethyl)-phenyl]-benzo[1,3]dioxol-5-yl}-ethanol
CAS NO:693219-96-4
Molecular Formula:
Molecular Weight: 450.486
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-{6-[2,3,4-trimethoxy-6-(2-methoxy-ethoxymethoxymethyl)-phenyl]-benzo[1,3]dioxol-5-yl}-ethanol(CAS DataBase Reference)
NIST Chemistry Reference: 1-{6-[2,3,4-trimethoxy-6-(2-methoxy-ethoxymethoxymethyl)-phenyl]-benzo[1,3]dioxol-5-yl}-ethanol(693219-96-4)
EPA Substance Registry System: 1-{6-[2,3,4-trimethoxy-6-(2-methoxy-ethoxymethoxymethyl)-phenyl]-benzo[1,3]dioxol-5-yl}-ethanol(693219-96-4)

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: 693219-96-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 693219-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,3,2,1 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 693219-96:
(8*6)+(7*9)+(6*3)+(5*2)+(4*1)+(3*9)+(2*9)+(1*6)=194
194 % 10 = 4
So 693219-96-4 is a valid CAS Registry Number.

693219-96-4Upstream product

693219-96-4Downstream Products

693219-96-4Relevant academic research and scientific papers

A Novel 1,3-Central-to-Axial Chirality Induction Approach to Cyclooctadiene Lignans

Baudoin, Olivier,Décor, Anne,Cesario, Michèle,Guéritte, Fran?oise

, p. 2009 - 2012 (2007/10/03)

The catalytic asymmetric synthesis of an axially chiral biaryl, potentially useful intermediate in the synthesis of dibenzocyclooctadiene lignans, has been performed. The key step consisted of a diastereoselective Suzuki coupling between a chiral benzylic

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