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Sigma-Aldrich

2,5-Dimethoxybenzene-1,4-dicarboxaldehyde

97%

Sinônimo(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

Fórmula empírica (Notação de Hill):
C10H10O4
Número CAS:
7310-97-6
Peso molecular:
194.18
Número MDL:
MFCD00017606
Código UNSPSC:
12352100
ID de substância PubChem:
329763336
NACRES:
NA.22

Ensaio

97%

forma

solid

pf

209-213 °C

cadeia de caracteres SMILES

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

chave InChI

YSIIHTHHMPYKFP-UHFFFAOYSA-N

Categorias relacionadas

Aplicação

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.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Certificados de análise (COA)

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2,5-DIMETHOXY-(1,4)BENZOQUINONE AldrichCPR

R164348

2,5-DIMETHOXY-(1,4)BENZOQUINONE

ANTHRACENE-2,3-DICARBOXALDEHYDE AldrichCPR

S100110

ANTHRACENE-2,3-DICARBOXALDEHYDE

Synthesis and Properties of Photoluminescent 1, 4-Bis-(alpha-cyano-4-methoxystyryl) benzenes
Loewe C, et al.
Synthesis, 2002, 1185-1190 (2002)
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
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
Shuting Zhuang et al.
Journal of hazardous materials, 385, 121596-121596 (2019-11-17)
Covalent organic frameworks (COFs) are emerging and promising adsorbents for the adsorptive removal of many types of pollutants. However, most COFs fabricated by various methods are in the form of microcrystalline powders, making them difficult in separation. In this study

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