Welcome to LookChem.com Sign In|Join Free
  • or
3,4,5-tris(hexyloxy)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156239-63-3

Post Buying Request

156239-63-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

156239-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156239-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,2,3 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156239-63:
(8*1)+(7*5)+(6*6)+(5*2)+(4*3)+(3*9)+(2*6)+(1*3)=143
143 % 10 = 3
So 156239-63-3 is a valid CAS Registry Number.

156239-63-3Relevant academic research and scientific papers

Impact of substitution pattern and chain length on the thermotropic properties of alkoxy-substituted triphenyl-tristriazolotriazines

Detert, Heiner,Glang, Stefan,Haspel, Tobias,Lehmann, Matthias,Limbach, Daniel,Rieth, Thorsten,Schupp, Niklas,Sperner, Marcel,Tober, Natalie,Wicker, Philipp

, (2021/06/14)

Tristriazolotriazines (TTTs) with a threefold alkoxyphenyl substitution were prepared and studied by DSC, polarized optical microscopy (POM) and X-ray scattering. Six pentyloxy chains are sufficient to induce liquid-crystalline behavior in these star-shap

Synthesis, Thermal, and Optical Properties of Tris(5-aryl-1,3,4-oxadiazol-2-yl)-1,3,5-triazines, New Star-Shaped Fluorescent Discotic Liquid Crystals

Tober, Natalie,Rieth, Thorsten,Lehmann, Matthias,Detert, Heiner

, p. 15295 - 15304 (2019/11/14)

The synthesis of tris(aryloxadiazolyl)triazines (TOTs), C3-symmetrical star-shaped mesogenes with a 1,3,5-triazine center, 5-phenyl-1,3,4-oxadiazole arms, and various peripheral alkoxy side chains is reported. Threefold Huisgen reaction on a ce

Bidirectional Association of Branched Noncovalent Complexes of Tetrazoles and 1,3,5-Tris(4,5-dihydroimidazol-2-yl)benzene in Solution

Kraft, Arno,Osterod, Frank,Froehlich, Roland

, p. 6425 - 6433 (2007/10/03)

Noncovalent 3:1 complexes were obtained by combining acidic tetrazoles with the tribasic 1,3,5-tris(4,5-dihydroimidazol-2-yl)benzene (1). A branched structure and the use of solubilizing groups ensured that the resulting complexes dissolved in a range of nonpolar organic solvents. An X-ray crystal structure analysis of a model complex with tetrazole showed a completely planar, C3-symmetrical, hydrogen-bonded molecule that salt-packed along the crystallographic c axis with an interplanar spacing of 3.31 A. Model binding studies between a tetrazolate and a protonated 1,3-bis(4,5-dihydroimidazol-2-yl)benzene allowed an association constant of 2470 ± 400 M-1 to be measured in the competitive solvent mixture CDCl3/CD3OD (97:3). The ionic nature and the extended planarity of the tetrazole complexes' core favored the formation of supramolecular stacks not only in the solid, but also in (nonpolar) solution. Self-association was evidenced by NMR and CD spectroscopy as well as by vapor-pressure osmometry.

Liquid Crystalline Primary Benzamides

Beginn, U.,Lattermann, G.

, p. 215 - 220 (2007/10/02)

Several alkoxybenzamides are synthesized and characterized by spectroscopic and chromatographic methods. 3,4,5-Tris(alkoxy)benzamides have been found to exhibit a mesophase of a columnar or stack-like type. - Keywords: liquid crystals, columnar phases, 3,

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 156239-63-3