Benzophenone-3,3′,4,4′-tetracarboxylic dianhydride(BTDA) - ≥99.5%, used for Used in the synthesis of polyimides. various applications , CAS No.2421-28-5

CAS: 2421-28-5 Cat. No.: B1507209 Formule: C₁₇H₆O₇ Poids moléculaire: 322.23 Beilstein Registry Number: 761777 Numéro CE: 219-348-1

GRADE & PURITY ≥99.5%

Storage

Room temperature,Argon charged

Shipped In

Normal

Vue d’ensemble

Benzophenone-3,3′,4,4′-tetracarboxylic acid is formed by hydrolysis, it can be converted to the dianhydride by treating with Ac2O (molar ratio 4 to 1 of acid).The dianhydride is used to synthesize polyimides, which are highly flexible in nature due to the presence of keto and carbonyl groups in the dianhydride molecule. The keto and carbonyl groups subsequently increase the spacing between the imide rings enhancing the solubility and processibility.

Specifications

Spécifications et pureté

≥99.5%

Application

Used in the synthesis of polyimides.

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

Normal

Pureté

≥99.5%

Noms et identifiants

Sourires canoniques

O=C(C1=CC2=C(C=C1)C(=O)OC2=O)C1=CC2=C(C=C1)C(=O)OC2=O

IUPAC Name

5,5'-Carbonyldi(2-benzofuran-1,3-dione)

InChIKey

VQVIHDPBMFABCQ-UHFFFAOYSA-N

INCHI

InChI=1S/C17H6O7/c18-13(7-1-3-9-11(5-7)16(21)23-14(9)19)8-2-4-10-12(6-8)17(22)24-15(10)20/h1-6H

Isomères SMILES

C1=CC2=C(C=C1C(=O)C3=CC4=C(C=C3)C(=O)OC4=O)C(=O)OC2=O

WGK Allemagne

1

Poids moléculaire

322.23

Beilstein

761777

Reaxy-Rn

761777

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=761777&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzophenones

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzophenones
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzophenones
• Alternative Parents: Tetracarboxylic acids and derivatives Phthalic anhydrides Isobenzofuranones Aryl ketones Carboxylic acid anhydrides Oxacyclic compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Benzophenone - Tetracarboxylic acid or derivatives - Phthalic_anhydride - Phthalic anhydride - Benzofuranone - Isobenzofuranone - Isocoumaran - Aryl ketone - Carboxylic acid anhydride - Ketone - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organic oxide - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl 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

Propriétés chimiques et physiques

• Solubilité: Soluble in DMF (0.1 g/mL). Reacts with water.Soluble in THF, Acetone
• Sensibilité: Moisture Sensitive
• Point d'éclair (°F): 615°F
• Point d'éclair (°C): 324°C
• Point d'ébullition (°C): 320°C/5mm
• Point de fusion (°C): 226°C