Tetrahydrofuran-2,3,4,5-tetracarboxylic Acid - ≥98%(T) , CAS No.26106-63-8

CAS: 26106-63-8 Cat. No.: T161756 Peso molecular: 248.14 Número EC: 247-461-6 PubChem CID: 97421

GRADE & PURITY ≥98%(T)

Synonyms

FT-0638573 | 2,5-anhydro-3,4-dicarboxy-3,4-dideoxyhexaric acid | UFOIOXZLTXNHQH-UHFFFAOYSA-N | DTXSID60948994 | D92427 | NSC 122277 | TETRAHYDROFURAN-2,3,4,5-TETRACARBOXYLICACID | C8H8O9 | T0975 | Tetrahydrofuran-2,3,4,5-tetracarboxylic Acid | 2,3,4,5-Fur

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

FT-0638573 | 2, 5-anhydro-3, 4-dicarboxy-3, 4-dideoxyhexaric acid | UFOIOXZLTXNHQH-UHFFFAOYSA-N | DTXSID60948994 | D92427 | NSC 122277 | TETRAHYDROFURAN-2, 3, 4, 5-TETRACARBOXYLICACID | C8H8O9 | T0975 | Tetrahydrofuran-2, 3, 4, 5-tetracarboxylic Acid | 2, 3, 4, 5-Fur

Especificaciones y pureza

≥98%(T)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(T)

Nombres e identificadores

• Pubchem Sid: 488187050
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187050
• Sonrisas canónicas: C1(C(C(OC1C(=O)O)C(=O)O)C(=O)O)C(=O)O
• IUPAC Name: oxolane-2,3,4,5-tetracarboxylic acid
• InChIKey: UFOIOXZLTXNHQH-UHFFFAOYSA-N
• INCHI: 1S/C8H8O9/c9-5(10)1-2(6(11)12)4(8(15)16)17-3(1)7(13)14/h1-4H,(H,9,10)(H,11,12)(H,13,14)(H,15,16)
• Isómeros SMILES: C1(C(C(OC1C(=O)O)C(=O)O)C(=O)O)C(=O)O
• PubChem CID: 97421
• Peso molecular: 248.14
• Reaxy-Rn: 1394540

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Tetracarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetracarboxylic acids and derivatives
• Alternative Parents: Tetrahydrofurans Oxacyclic compounds Dialkyl ethers Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Tetracarboxylic acid or derivatives - Tetrahydrofuran - Oxacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
• Descripción: 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

Objetivos asociados (humanos)

GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)

Discover Target: GNAS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Punto de fusión (°C): 205℃
• Peso molecular: 248.140 g/mol
• XLogP3: -1.800
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 4
• Exact Mass: 248.017 Da
• Monoisotopic Mass: 248.017 Da
• Topological Polar Surface Area: 158.000 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 350.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 4
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1