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"3,6,9,12,15,18,21,24,27,30,33,36,39,42,45,48,51-heptadecaoxa-tripentacontane-1,53-diol" is a complex organic compound characterized by its unique molecular structure. It is a long-chain molecule composed of 36 carbon atoms, with 17 oxygen atoms incorporated into the chain, forming ether (C-O-C) linkages. The compound is named based on the positions of the oxygen atoms along the carbon chain, which are at the 3rd, 6th, 9th, and so on, up to the 51st carbon atom. The "1,53-diol" part of the name indicates that there are two hydroxyl (-OH) groups attached to the first and 53rd carbon atoms, respectively. 3,6,9,12,15,18,21,24,27,30,33,36,39,42,45,48,51-heptadecaoxa-tripentacontane-1,53-diol is an example of a polyether, which is known for its ability to form strong complexes with metal ions, and it may have applications in various fields such as chemistry, materials science, and potentially as a chelating agent in industrial processes.

4445-03-8

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4445-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4445-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4445-03:
(6*4)+(5*4)+(4*4)+(3*5)+(2*0)+(1*3)=78
78 % 10 = 8
So 4445-03-8 is a valid CAS Registry Number.

4445-03-8Downstream Products

4445-03-8Relevant academic research and scientific papers

Preparation and crystallinity of a large unsubstituted crown ether, cyclic heptacosa(oxyethylene) (cyclo-E27, 81-crown-27), studied by Raman spectroscopy, X-ray scattering and differential scanning calorimetry

Yang, Zhuo,Yu, Ga-Er,Cooke, Jennifer,Ali-Adib, Ziad,Viras, Kyriakos,Matsuura, Hiroatsu,Ryan, Anthony J.,Booth, Colin

, p. 3173 - 3182 (2007/10/03)

Cyclic heptacosa(oxyethyelene) (cyclo-E27, 81-crown-27) was prepared from linear α-hydro, ω-hydroxy-heptacosa(oxyethylene) by reaction with tosyl chloride under alkaline conditions, purified by preparative-scale gel permeation chromatography, and studied by laser-Raman spectroscopy, wide-angle and small-angle X-ray scattering, and differential scanning calorimetry. Comparison was made with the properties of linear oligo(oxyethylene) dimethyl ethers (including C1E27C1). The sub-cell of the crystalline cyclic oligomer was the same as that of its linear counterparts, i.e. the same as that of high-molar-mass poly(oxyethylene). However, the cyclic oligomer crystallised as a twice-folded ring, as confirmed by its long spacing and the frequency of its single-node longitudinal acoustic mode (LAM-1). Enthalpies of fusion and melting temperatures were analysed to provide estimates of the enthalpy and entropy of formation of a fold in an oligo(oxyethylene) layer crystal.

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