2,5-Dimethoxybenzene-1,4-dicarboxaldehyde - ≥97% , CAS No.7310-97-6

CAS: 7310-97-6 Cat. No.: B300494 Molecular Weight: 194.18 EC Number: 623-127-9

GRADE & PURITY ≥97%

Synonyms

YSZC304 | MFCD00017606 | 2,5-Dimethoxyterephthalaldehyde | DMTP | DMA

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Overview

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.

Specifications

Synonyms

YSZC304 | MFCD00017606 | 2, 5-Dimethoxyterephthalaldehyde | DMTP | DMA

Specifications & Purity

≥97%

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 504759507
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504759507
• Canonical Smiles: COC1=CC(=C(C=C1C=O)OC)C=O
• IUPAC Name: 2,5-dimethoxyterephthalaldehyde
• InChIKey: YSIIHTHHMPYKFP-UHFFFAOYSA-N
• INCHI: 1S/C10H10O4/c1-13-9-3-8(6-12)10(14-2)4-7(9)5-11/h3-6H,1-2H3
• Isomeric SMILES: COC1=CC(=C(C=C1C=O)OC)C=O
• Molecular Weight: 194.18
• Reaxy-Rn: 515699
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=515699&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Methoxybenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Methoxybenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Dimethoxybenzenes
• Alternative Parents: Phenoxy compounds Benzoyl derivatives Benzaldehydes Anisoles Alkyl aryl ethers Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Dimethoxybenzene - P-dimethoxybenzene - Anisole - Benzaldehyde - Benzoyl - Phenol ether - Phenoxy compound - Aryl-aldehyde - Alkyl aryl ether - Ether - Organooxygen compound - Aldehyde - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as dimethoxybenzenes. These are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Air sensitive
• Melt Point(°C): 209-213 °C
• Molecular Weight: 194.180 g/mol
• XLogP3: 0.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 194.058 Da
• Monoisotopic Mass: 194.058 Da
• Topological Polar Surface Area: 52.600 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 182.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

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