Cas 241488-03-9,bis-(3,4-dimethoxy-phenyl)-[2-(2-methyl-[1,3]dioxolan-2-yl)-phenyl]-methanol

241488-03-9

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Basic information

Product Name: bis-(3,4-dimethoxy-phenyl)-[2-(2-methyl-[1,3]dioxolan-2-yl)-phenyl]-methanol
Synonyms: bis-(3,4-dimethoxy-phenyl)-[2-(2-methyl-[1,3]dioxolan-2-yl)-phenyl]-methanol
CAS NO:241488-03-9
Molecular Formula:
Molecular Weight: 466.531
EINECS: N/A
Product Categories: N/A
Mol File: 241488-03-9.mol
Article Data: 1

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: bis-(3,4-dimethoxy-phenyl)-[2-(2-methyl-[1,3]dioxolan-2-yl)-phenyl]-methanol(CAS DataBase Reference)
NIST Chemistry Reference: bis-(3,4-dimethoxy-phenyl)-[2-(2-methyl-[1,3]dioxolan-2-yl)-phenyl]-methanol(241488-03-9)
EPA Substance Registry System: bis-(3,4-dimethoxy-phenyl)-[2-(2-methyl-[1,3]dioxolan-2-yl)-phenyl]-methanol(241488-03-9)

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: 241488-03-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 241488-03-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,1,4,8 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 241488-03:
(8*2)+(7*4)+(6*1)+(5*4)+(4*8)+(3*8)+(2*0)+(1*3)=129
129 % 10 = 9
So 241488-03-9 is a valid CAS Registry Number.

241488-03-9Upstream product

241488-03-9Downstream Products

241488-03-9Relevant articles and documents

Synthesis of a stable mimic for the ring closed form of gallein, featuring a novel one pot boron tribromide mediated intramolecular cyclisation process

Crew, Andrew P. A.,Lyons, Amanda J.,Camp, Nicholas P.

, p. 1133 - 1135 (2007/10/03)

Treatment of 9-{2-[1-(1,3-dioxalan-2-yl)ethyl]phenyl}-3,4,5,6-tetrabenzyloxy-9H-xanthen-9-o l 14 with excess boron tribromide at -78°C, and warming to room temperature, provides a facile route to 3,4,5,6-tetrahydroxy-spiro(1H-indene-1,9-[9H]-xanthene-3-(2

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