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methyl 3,4,5-triethoxybenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39666-77-8

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39666-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39666-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,6 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39666-77:
(7*3)+(6*9)+(5*6)+(4*6)+(3*6)+(2*7)+(1*7)=168
168 % 10 = 8
So 39666-77-8 is a valid CAS Registry Number.

39666-77-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3,4,5-triethoxybenzoate

1.2 Other means of identification

Product number -
Other names 3,4,5-triethoxy-benzoic acid methyl ester

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:39666-77-8 SDS

39666-77-8Relevant academic research and scientific papers

DIARYL TREHALOSE COMPOUNDS AND USES THEREOF

-

Paragraph 00262, (2019/09/12)

Disclosed herein are diaryl trehalose compounds and methods of use thereof, for example as vaccine adjuvants.

Synthesis and properties of hole-transporting triphenylamine-derived dendritic compounds

Reghu, Renji R.,Simokaitiene, Jurate,Grazulevicius, Juozas V.,Raisys, Steponas,Kazlauskas, Karolis,Jursenas, Saulius,Jankauskas, Vygintas,Reina, Antonio

, p. 135 - 142 (2015/03/05)

Materials based on triphenylamino core linked with different alkoxyphenyl-substituents through olefinic spacers were synthesised, and their thermal, photophysical and photoelectrical properties were investigated. The synthesized compounds showed relativel

Influence of alkoxy tail length on the phase behaviour of mesogen-jacketed liquid crystalline polymers with fan-shaped pendants

Yang, Chang-An,Wang, Guo,Xie, He Lou,Zhang, Hai Liang

experimental part, p. 4503 - 4510 (2011/11/06)

A series of new monomers of 2, 5-bis [(3, 4, 5-trialkoxy benzyl) oxycarbonyl] styrene (denoted as M-tri-OCmH2m + 1, m = 1, 2, 4, 6, 8, 10, 12, where m indicated the number of carbon atoms in the alkoxy group) were designed and synthesized. Then, their corresponding polymers P-tri-OCmH2m + 1 (m = 1, 2, 4, 6, 8, 10, 12) were synthesized by free radical polymerization. The chemical structure of the monomers was confirmed by elemental analysis, 1H NMR and 13C NMR. The molecular characterization of polymers was performed with 1H NMR, gel permeation chromatography (GPC). The thermal stability of polymers was investigated by thermogravimetric analysis (TGA). The phase structure and transition behaviours were studied using differential scanning calorimetry (DSC), polarized light microscopy (PLM), one- and two-dimensional (1D and 2D) wide-angle X-ray diffraction (WAXD). We found that P-tri-OCmH2m + 1 (m = 1, 2) with short n-alkoxy substituents as the tail form columnar nematic (ΦN) phase; that with the increasing length of alkoxy tails, P-tri-OCmH2m + 1 (m = 4, 6, 8) can demonstrate the hexagonal columnar (ΦH) phase; however, when the length of alkoxy tails exceeded a threshold, P-tri-OCmH2m + 1 (m = 10, 12) only develop into columnar nematic (ΦN) phase instead of ΦH phase.

Molecular control of macroscopic cubic, columnar, and lamellar organizations in luminescent lanthanide-containing thermotropic liquid crystals

Terazzi, Emmanuel,Torelli, Stephane,Bernardinelli, Gerald,Rivera, Jean-Pierre,Benech, Jean-Marc,Bourgogne, Cyril,Donnio, Bertrand,Guillon, Daniel,Imbert, Daniel,Buenzli, Jean-Claude G.,Pinto, Andre,Jeannerat, Damien,Piguet, Claude

, p. 888 - 903 (2007/10/03)

The connection of lipophilic gallic acid derivatives at the 5,5′- or 6,6′-positions of the rigid 2,6-bis(1-ethyl-benzimidazol-2-yl)pyridine core provides two pro-mesogenic tridentate ligands L10 and L12, whose molecular shapes, anisometries, and directional intermolecular π-stacking can be tuned. X-ray diffraction data in the crystalline state, combined with solution 1H NMR measurements, show that complexation with trivalent lanthanides, Ln(III), produces the neutral hemi-disklike complexes [Ln(Li)(NO3)3] (i = 10, 12), which dimerize to give the rodlike bimetallic complexes [Ln2(Li)2(NO 3)6] at lower temperature. The relevant thermodynamic parameters for the latter process depend on the nature of the ligand, the size of the metal ion, and the strength of the intermolecular interactions involved in the condensed phase. These three-dimensional models obtained for the complexes in the crystals and in solution are eventually confronted with small-angle XRD profiles recorded in the intermediate thermotropic liquid crystalline phase, in which the rigidity of the packed polyaromatic cores is maintained, while the alkyl chains are molten. According to the specific geometries and nuclearities of the molecular complexes, three types of mesophases (lamellar, columnar, and cubic) can be induced, which provides a direct correlation between the microscopic arrangements and the macroscopic ordering in lanthanide-containing metallomesogens.

Depigmenting activity and low cytotoxicity of alkoxy benzoates or alkoxy cinnamte in cultured melanocytes

Kang, Hak Hee,Rho, Ho Sik,Hwang, Jae Sung,Oh, Seong-Geon

, p. 1085 - 1088 (2007/10/03)

To obtain effective and safe topical depigmenting agents, we synthesized hydroxybenzoates, alkoxybenzoates, and 3,4,5-trimethoxycinnamate containing a thymol moiety and screened then for high-level inhibitory activity against melanin synthesis in cultured melanocytes. Eight compounds were tested for their depigmenting effect and cytotoxicity using a murine melanocyte cell line. We found that 3,4,5-trialkoxybenzoates and 3,4,5-trimethoxycinnamate, synthesized by conjugating 3,4,5-trialkoxybenzoic acids and 3,4,5-trimethoxycinnmic acid with thymol, showed a potent depigmenting effect and low cytotoxicity. Compound 4h, 5-methyl-2-(methylethyl)phenyl (2E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate, showed the most potent depigmenting effect (IC50=10 μM) with low cytotoxicity (IC50=200 μM).

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