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15403-46-0

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15403-46-0 Usage

General Description

2,5-Diaminoterephthalic acid diethyl ester is a chemical compound with the molecular formula C14H18N2O4. It is a diethyl ester derivative of 2,5-diaminoterephthalic acid, which is used in the production of various polymers. 2,5-Diaminoterephthalic acid diethyl ester is commonly used in the synthesis of functionalized polymers and as a monomer for the preparation of metal-organic frameworks. It is also used as a crosslinking agent in the production of polymers and as a ligand for coordinating metal ions in coordination complexes. Additionally, it has potential applications in the fields of catalysis, gas storage, and drug delivery systems.

Check Digit Verification of cas no

The CAS Registry Mumber 15403-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,0 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15403-46:
(7*1)+(6*5)+(5*4)+(4*0)+(3*3)+(2*4)+(1*6)=80
80 % 10 = 0
So 15403-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O4/c1-3-17-11(15)7-5-10(14)8(6-9(7)13)12(16)18-4-2/h5-6H,3-4,13-14H2,1-2H3

15403-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2,5-diaminobenzene-1,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2,5-diamino-terephthalic acid diethyl 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:15403-46-0 SDS

15403-46-0Relevant articles and documents

Bis-silylated terephthalate as a building block precursor for highly fluorescent organic-inorganic hybrid materials

Pletsch, Daniela,Da Silveira Santos, Fabiano,Rodembusch, Fabiano Severo,Stefani, Valter,Campo, Leandra Franciscato

, p. 2506 - 2513 (2013/02/25)

A bis-silylated diethyl 2,5-bis[N,N-(3-triethoxysilyl)propylurea] terephthalate precursor (5) was synthesized from a terephthalate derivative (3) and successfully used to prepare highly fluorescent organosilicas by hydrolytic self-condensation (DPM1) and co-condensation (DPM2) with tetraethoxysilane. The dyes 3 and 5 present absorption in the UV-Vis region and fluorescence emission in the yellow and blue regions, respectively. The red-shifted bands in the absorption spectra of dye 3 with respect to dye 5 can be related to the formation of intramolecular charge transfer (ICT) state even in the ground-state due to the strong electron-donor amino groups and moderate electron-withdrawing carbonyl groups present in the benzenic ring. The small Stokes' shift, as well as the high fluorescence quantum yield values discards the intramolecular proton transfer mechanism in the excited state. The fluorescence emission dependence on the solvent polarity indicates that an intramolecular charge transfer (ICT) or a locally excited (LE) state is taking place in the excited state to the dyes 3 and 5, respectively. The new fluorescent hybrid materials (DPM1 and DPM2) show absorption maxima in the solid state located at around 390 nm, indicating that the electronic structure of the fluorescent precursor was not significantly perturbed in the ground state after its self-condensation or co-condensation with TEOS. The fluorescent material DPM2 presents a photophysical behavior quite similar to the precursor in solution. On the other hand, the self-condensed material DPM1 presents a fluorescence emission maximum red-shifted by 33 nm, which can be probably attributed to π-π stacking between the terephthalate cores. Any evidence of auto-organization could be observed in these materials. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2012.

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