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715026

2,5-Dimethoxybenzene-1,4-dicarboxaldehyde

Name: 2,5-Dimethoxybenzene-1,4-dicarboxaldehyde
Brand: ALDRICH

97%

Synonym(s):

2,5-Dimethoxy-1,4-benzenedialdehyde, 2,5-Dimethoxy-1,4-benzenedicarboxaldehyde, 2,5-Dimethoxy-4-formylbenzaldehyde, 2,5-Dimethoxybenzene-1,4-dicarbaldehyde, 2,5-Dimethoxyterephthalaldehyde, 2,5-Dimethoxyterephthaldehyde

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₁₀O₄

CAS Number:

7310-97-6

Molecular Weight:

194.18

NACRES:

NA.22

PubChem Substance ID:

329763336

UNSPSC Code:

12352100

MDL number:

MFCD00017606

Assay:

97%

Form:

solid

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Properties

Quality Level

100

assay

97%

form

solid

mp

209-213 °C

functional group

aldehyde

SMILES string

COc1cc(C=O)c(OC)cc1C=O

InChI

1S/C10H10O4/c1-13-9-3-8(6-12)10(14-2)4-7(9)5-11/h3-6H,1-2H3

InChI key

YSIIHTHHMPYKFP-UHFFFAOYSA-N

Description

Application

2,5-Dimethoxybenzene-1,4-dicarboxaldehyde can be used as a reactant to synthesize:

Polymeric Schiff bases using aliphatic or aromatic diamines via polycondensation reaction.
1,4-Bis-(α-cyano-4-methoxystyryl)-2,5-dimethoxybenzene using (4-methoxyphenyl)acetonitrile via Knoevenagel reaction in the presence of potassium t-butoxide and tetrabutylammonium hydroxide.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Spherical mesoporous covalent organic framework as a solid-phase extraction adsorbent for the ultrasensitive determination of sulfonamides in food and water samples by liquid chromatography-tandem mass spectrometry.

Lian Wen et al.

Journal of chromatography. A, 1625, 461275-461275 (2020-07-28)

Efficient extraction of polar sulfonamides antibiotics from aqueous samples and food is very challenging, because they are hydrophilic, their concentration is very low, and the matrix is complex. Covalent organic frameworks (COFs), a novel porous organic material, have attracted great

Synthesis and Properties of Photoluminescent 1, 4-Bis-(alpha-cyano-4-methoxystyryl) benzenes

Loewe C, et al.

Synthesis, 2002, 1185-1190 (2002)

Polymeric Schiff bases as low-voltage redox centers for sodium-ion batteries.

Elizabeth Castillo-Martínez et al.

Angewandte Chemie (International ed. in English), 53(21), 5341-5345 (2014-04-24)

The redox entity comprising two Schiff base groups attached to a phenyl ring (-N=CH-Ar-HC=N-) is reported to be active for sodium-ion storage (Ar=aromatic group). Electroactive polymeric Schiff bases were produced by reaction between non-conjugated aliphatic or conjugated aromatic diamine block

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Global Trade Item Number

SKU	GTIN
715026-1G	04061832848808