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

17920-89-7

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17920-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17920-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,2 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17920-89:
(7*1)+(6*7)+(5*9)+(4*2)+(3*0)+(2*8)+(1*9)=127
127 % 10 = 7
So 17920-89-7 is a valid CAS Registry Number.

17920-89-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names -

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:17920-89-7 SDS

17920-89-7Downstream Products

17920-89-7Relevant academic research and scientific papers

Transport of sodium, potassium, calcium and magnesium ions through liquid membrane containing non-cyclic ionophores composed of furan units

Asrani, Loni,Sharma, Uma

, p. 176 - 177 (2007/10/02)

2,2-Difurylpropane (IB) and 2,5-bis(dimethylfurfuryl) furan (IIB) have been synthesized by the condensation of furan and acetone in ethanol in the presence of conc.HCl.These oligomers exhibit the ability to transport alkali and alkaline earth metal ions through chloroform membrane and are selective for sodium and magnesium ions.Transport of alkali metal ions is relatively more facile than that of alkaline earth cations.Selectivity for Na+/K+ is reduced when a mixture of cations is used.These carriers are highly selective for the pair Na+/Mg2+ compared to the pair K+/Ca2+.

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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