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Furan, 2,2'-(1-methylethylidene)bis[5-[1-(2-furanyl)-1-methylethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61093-48-9

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61093-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61093-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,9 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61093-48:
(7*6)+(6*1)+(5*0)+(4*9)+(3*3)+(2*4)+(1*8)=109
109 % 10 = 9
So 61093-48-9 is a valid CAS Registry Number.

61093-48-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(furan-2-yl)propan-2-yl]-5-[2-[5-[2-(furan-2-yl)propan-2-yl]furan-2-yl]propan-2-yl]furan

1.2 Other means of identification

Product number -
Other names Furan,2,2'-(1-methylethylidene)bis[5-[1-(2-furanyl)-1-methylethyl]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61093-48-9 SDS

61093-48-9Relevant academic research and scientific papers

Syntheses of Tetraoxaquaterene Derivatives

Tanaka, Sanae,Tomokuni, Hidehiko

, p. 991 - 994 (2007/10/02)

Several new dimethyl and tetramethyl tetraoxaquaterenes, 3d and 3e, have been prepared in order to synthesize the oxygen analogues of porphyrin.The reaction between furan and a ketone using an acidic catalyst gave the cyclic tetramer, tetraquaterene, and oligomers.On the other hand, in the case of furan and the aldehyde, only linear oligomers were isolated.The condensation of furan-containing dimers with carbonyl compounds, both ketone and aldehyde, except formaldehyde, gave the tetraoxaquaterene.In the case of formaldehyde, the yield of cyclic tetramer was neglijable.

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