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1,4,7,10,13-Pentaoxacyclopentadecane, 2-[(2-methoxyphenoxy)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76719-75-0

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76719-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76719-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,1 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76719-75:
(7*7)+(6*6)+(5*7)+(4*1)+(3*9)+(2*7)+(1*5)=170
170 % 10 = 0
So 76719-75-0 is a valid CAS Registry Number.

76719-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-((2-methoxyphenoxy)methyl)-15-crown-5

1.2 Other means of identification

Product number -
Other names [(2-methoxyphenoxy)methyl]-15-crown-5

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:76719-75-0 SDS

76719-75-0Downstream Products

76719-75-0Relevant academic research and scientific papers

Crystallographic evidence of side-arm lariat effect in the series of chiral ortho- and para-methoxyphenoxymethyl-15-crown-5 complexes with sodium perchlorate

Bredikhin, Alexander A.,Gubaidullin, Aidar T.,Bredikhina, Zemfira A.,Fayzullin, Robert R.

, p. 176 - 184 (2013/02/23)

The single crystals of the NaClO4 complexes with two potential lariat 15-crowns-5 having ortho- or para-methoxyphenoxymethyl side arms were investigated by X-ray analysis in racemic and enantiopure form. Only ortho-derivative demonstrates laria

Crown Cation Complex Effects. 20. Syntheses and Cation Binding Properties of Carbon-Pivot Lariat Ethers

Dishong, Dennis M.,Diamond, Craig J.,Cinoman, Michael I.,Gokel, Geoge W.

, p. 586 - 593 (2007/10/02)

In an effort devise synthetic cation binders that will mimic the behavior of naturally occuring ionophores such as valinomycin, we have prepared approximately 30 macrocyclic (crown) polyethers bearing flexible side chains attached to the macro ring at carbon.In many of these "carbon-pivot" compounds, the side chain contains one or more neutral donor groups that, if in a suitable geometrical arrangement, may provide additional solvation to the macro-ring-bound cation.Although such donors often enhanced the cation binding ability, overall, the increases in stability constants were modest.The physical resemblance and concept of "roping and tying" the cation suggest the name "lariat ethers".Syntheses of these molecules and binding by them of Na+ and K+ cations are reported and conclusions drawn about the structural requirements and cation binding efficacy of these materials.

Lariat Ethers. Synthesis and Cation Binding of Macrocyclic Polyethers Possessing Axially Disposed Secondary Donor Groups

Gokel, George W.,Dishong, Dennis M.,Diamond, Craig J.

, p. 1053 - 1054 (2007/10/02)

The synthesis and cation binding properties of a series of macrocyclic polyethers which possess ligating arms that enhance cation binding is presented.

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