3,3',4,4'-Diphenylsulfonetetracarboxylic Dianhydride(DSDA) - ≥99%(HPLC),purified by sublimation , CAS No.2540-99-0

CAS: 2540-99-0 Cat. No.: D155088 Molecular Weight: 358.28 Beilstein Registry Number: 18(5)3,189 EC Number: 807-101-6

GRADE & PURITY ≥99%(HPLC), purified by sublimation

Synonyms

3,3',4,4'-Diphenylsulfone tetracarboxylic dianhydride | EC 807-101-6 | MFCD00039145 | 3,3',4,4'-Diphenyl sulfone tetracarboxylic anhydride | SY054994 | 3,3 inverted exclamation mark ,4,4 inverted exclamation mark -Diphenylsulfonetetracarboxylic Dianhydrid

Storage

Room temperature,Argon charged,Desiccated,Cool

Shipped In

Normal

Specifications

Synonyms

3, 3', 4, 4'-Diphenylsulfone tetracarboxylic dianhydride | EC 807-101-6 | MFCD00039145 | 3, 3', 4, 4'-Diphenyl sulfone tetracarboxylic anhydride | SY054994 | 3, 3 inverted exclamation mark , 4, 4 inverted exclamation mark -Diphenylsulfonetetracarboxylic Dianhydrid

Specifications & Purity

≥99%(HPLC), purified by sublimation

Storage

Room temperature, Argon charged, Desiccated, Cool

Shipped In

Normal

Purity

≥99%(HPLC)

Names and Identifiers

• Pubchem Sid: 504754979
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754979
• Canonical Smiles: C1=CC2=C(C=C1S(=O)(=O)C3=CC4=C(C=C3)C(=O)OC4=O)C(=O)OC2=O
• IUPAC Name: 5-[(1,3-dioxo-2-benzofuran-5-yl)sulfonyl]-2-benzofuran-1,3-dione
• InChIKey: ZHBXLZQQVCDGPA-UHFFFAOYSA-N
• INCHI: 1S/C16H6O8S/c17-13-9-3-1-7(5-11(9)15(19)23-13)25(21,22)8-2-4-10-12(6-8)16(20)24-14(10)18/h1-6H
• Isomeric SMILES: C1=CC2=C(C=C1S(=O)(=O)C3=CC4=C(C=C3)C(=O)OC4=O)C(=O)OC2=O
• Molecular Weight: 358.28
• Beilstein: 18(5)3,189
• Reaxy-Rn: 1298403
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1298403&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Tetracarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Tetracarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetracarboxylic acids and derivatives
• Alternative Parents: Phthalic anhydrides Isobenzofuranones Benzenoids Sulfones Carboxylic acid anhydrides Oxacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Tetracarboxylic acid or derivatives - Phthalic_anhydride - Phthalic anhydride - Benzofuranone - Isobenzofuranone - Isocoumaran - Benzenoid - Carboxylic acid anhydride - Sulfonyl - Sulfone - Oxacycle - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organic oxide - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl 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

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ACHN (49357 Activities)

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Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Moisture sensitive.
• Melt Point(°C): 283°C(lit.)
• Molecular Weight: 358.300 g/mol
• XLogP3: 1.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 2
• Exact Mass: 357.978 Da
• Monoisotopic Mass: 357.978 Da
• Topological Polar Surface Area: 129.000 Ų
• Heavy Atom Count: 25
• Formal Charge: 0
• Complexity: 705.000
• 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

References

1. Peiyuan Zuo, Jinpeng Li, Donglin Chen, Lingzhi Nie, Liang Gao, Jingyu Lin, Qixin Zhuang.  (2023)  Scalable co-cured polyimide/poly(p-phenylene benzobisoxazole) all-organic composites enabling improved energy storage density, low leakage current and long-term cycling stability.  Materials Horizons,  11  (1): (271-282).  [PMID:37938919] [10.1039/D3MH01479G]

2. Jianing Zhang, Jian Zhou, Yuanpeng Deng, Hongxuan Yu, Han Zhao, Jingran Guo, Pengyu Zhang, Shixuan Dang, Dizhou Liu, Duola Wang, Yingde Zhao, Chuanyun Song, Cong Li, Zhengli Yan, Jiali Chen, Hui Li, Xiang Xu.  (2024)  Self-contact-electrification aerogel for all-in-one triboelectricity generation.  Nano Energy,      [PMID:] [10.1016/j.nanoen.2024.109693]

3. Shuo Lv, Mingzu Zhang, Jinlin He, Peihong Ni.  (2024)  Tri-monomer polyamide acid nanofiber separator for safe and high performance lithium-ion batteries.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2024.134621]